Canonical Allele Identifier: CA2525615849

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71745940C>G , CM000666.2:g.71745940C>G	GRCh38
NC_000004.11:g.72611657C>G , CM000666.1:g.72611657C>G	GRCh37
NC_000004.10:g.72830521C>G	NCBI36
NG_012837.2:g.64581G>C
NG_012837.3:g.64581G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.*25+211G>C MANE Select	ENSP00000273951.8:n.*25+211G>C
ENST00000273951.12:c.*25+211G>C	ENSP00000273951.8:n.*25+211G>C
ENST00000503364.5:n.123+211G>C
ENST00000503472.5:n.1334+211G>C
ENST00000504199.5:c.*25+211G>C	ENSP00000421725.1:n.*25+211G>C
ENST00000509740.5:c.*273+211G>C	ENSP00000422664.1:n.*273+211G>C
ENST00000513476.5:c.1396-4070G>C	ENSP00000426683.1:n.1396-4070G>C
NM_000583.3:c.*25+211G>C	NP_000574.2:n.*25+211G>C
NM_001204306.1:c.*25+211G>C	NP_001191235.1:n.*25+211G>C
NM_001204307.1:c.*25+211G>C	NP_001191236.1:n.*25+211G>C
XM_006714177.2:c.*39+211G>C	XP_006714240.1:n.*39+211G>C
XM_006714177.3:c.*39+211G>C	XP_006714240.1:n.*39+211G>C
NM_000583.4:c.*25+211G>C MANE Select	NP_000574.2:n.*25+211G>C