Canonical Allele Identifier: CA357199272
Gene: GC HGNC NCBI

Linked Data

dbSNP Id: rs1560685615

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71741858C>A , CM000666.2:g.71741858C>A GRCh38
NC_000004.11:g.72607575C>A , CM000666.1:g.72607575C>A GRCh37
NC_000004.10:g.72826439C>A NCBI36
NG_012837.2:g.68663G>T
NG_012837.3:g.68663G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000273951.13:c.*38G>T MANE Select ENSP00000273951.8:n.*38G>T
ENST00000273951.12:c.*38G>T ENSP00000273951.8:n.*38G>T
ENST00000503364.5:n.136G>T
ENST00000503472.5:n.1347G>T
ENST00000504199.5:c.*38G>T ENSP00000421725.1:n.*38G>T
ENST00000509740.5:c.*286G>T ENSP00000422664.1:n.*286G>T
ENST00000513476.5:c.1408G>T ENSP00000426683.1:p.Ala470Ser
NM_000583.3:c.*38G>T NP_000574.2:n.*38G>T
NM_001204306.1:c.*38G>T NP_001191235.1:n.*38G>T
NM_001204307.1:c.*38G>T NP_001191236.1:n.*38G>T
XM_006714177.2:c.*52G>T XP_006714240.1:n.*52G>T
XM_006714177.3:c.*52G>T XP_006714240.1:n.*52G>T
NM_000583.4:c.*38G>T MANE Select NP_000574.2:n.*38G>T