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 17:4899036 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM004693

Most severe consequence
Clinical significance

This variation has 4 HGVS names - click the plus to show

17:g.4899036C>G
ENST00000572438.1:n.977G>C
ENST00000293780.4:c.1291G>C
ENSP00000293780.4:p.Ala431Pro

Variation displays