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 5:37002734 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM042511

Most severe consequence
Clinical significance

Synonyms

LSDB 15886

This variation has 6 HGVS names - click the plus to show

5:g.37002734C>G
ENST00000448238.2:c.3737C>G
ENSP00000406266.2:p.Ala1246Gly
ENST00000621733.1:c.1-61844C>G
ENST00000282516.10:c.3737C>G
ENSP00000282516.8:p.Ala1246Gly

Variation displays