Canonical Allele Identifier: CA357212465

Gene: GC

Linked Data

• COSMIC: COSM1594575
• MyVariant Identifiers: chr4:g.72649738T>C (hg19) ; chr4:g.71784021T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71784021T>C , CM000666.2:g.71784021T>C	GRCh38
NC_000004.11:g.72649738T>C , CM000666.1:g.72649738T>C	GRCh37
NC_000004.10:g.72868602T>C	NCBI36
NG_012837.2:g.26500A>G
NG_012837.3:g.26500A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.-3A>G MANE Select	ENSP00000273951.8:n.-3A>G
ENST00000273951.12:c.-3A>G	ENSP00000273951.8:n.-3A>G
ENST00000504199.5:c.55A>G	ENSP00000421725.1:p.Lys19Glu
ENST00000506245.1:c.-3A>G	ENSP00000426718.1:n.-3A>G
ENST00000509740.5:c.-3A>G	ENSP00000422664.1:n.-3A>G
ENST00000513476.5:c.-3A>G	ENSP00000426683.1:n.-3A>G
NM_000583.3:c.-3A>G	NP_000574.2:n.-3A>G
NM_001204306.1:c.-3A>G	NP_001191235.1:n.-3A>G
NM_001204307.1:c.55A>G	NP_001191236.1:p.Lys19Glu
XM_006714177.2:c.-3A>G	XP_006714240.1:n.-3A>G
XM_006714177.3:c.-3A>G	XP_006714240.1:n.-3A>G
NM_000583.4:c.-3A>G MANE Select	NP_000574.2:n.-3A>G