Canonical Allele Identifier: CA357212364

Gene: GC

Linked Data

• MyVariant Identifiers: chr4:g.72649728C>G (hg19) ; chr4:g.71784011C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71784011C>G , CM000666.2:g.71784011C>G	GRCh38
NC_000004.11:g.72649728C>G , CM000666.1:g.72649728C>G	GRCh37
NC_000004.10:g.72868592C>G	NCBI36
NG_012837.2:g.26510G>C
NG_012837.3:g.26510G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.8G>C MANE Select	ENSP00000273951.8:p.Arg3Thr
ENST00000273951.12:c.8G>C	ENSP00000273951.8:p.Arg3Thr
ENST00000504199.5:c.65G>C	ENSP00000421725.1:p.Arg22Thr
ENST00000506245.1:c.8G>C	ENSP00000426718.1:p.Arg3Thr
ENST00000509740.5:c.8G>C	ENSP00000422664.1:p.Arg3Thr
ENST00000513476.5:c.8G>C	ENSP00000426683.1:p.Arg3Thr
NM_000583.3:c.8G>C	NP_000574.2:p.Arg3Thr
NM_001204306.1:c.8G>C	NP_001191235.1:p.Arg3Thr
NM_001204307.1:c.65G>C	NP_001191236.1:p.Arg22Thr
XM_006714177.2:c.8G>C	XP_006714240.1:p.Arg3Thr
XM_006714177.3:c.8G>C	XP_006714240.1:p.Arg3Thr
NM_000583.4:c.8G>C MANE Select	NP_000574.2:p.Arg3Thr