Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

Chromosome 17:75278265 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM022068

Most severe consequence
Clinical significance

Synonyms

LSDB 13877

This variation has 17 HGVS names - click the plus to show

17:g.75278265C>G
ENST00000580273.1:c.227G>C
ENSP00000463039.1:p.Gly76Ala
ENST00000320362.4:c.530G>C
ENSP00000319574.3:p.Gly177Ala
ENST00000580994.2:c.530G>C
ENSP00000463795.1:p.Gly177Ala
ENST00000416858.3:c.530G>C
ENSP00000397818.2:p.Gly177Ala
ENST00000402418.4:c.530G>C
ENSP00000385312.3:p.Gly177Ala
ENST00000375261.5:c.359G>C
ENSP00000364410.4:p.Gly120Ala
ENST00000582822.1:c.152-4977G>C
ENST00000442286.3:c.530G>C
ENSP00000402202.2:p.Gly177Ala
ENST00000583332.2:c.460-4626G>C

Variation displays