Canonical Allele Identifier: CA357204929

Gene: GC

Linked Data

• MyVariant Identifiers: chr4:g.72622566A>C (hg19) ; chr4:g.71756849A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71756849A>C , CM000666.2:g.71756849A>C	GRCh38
NC_000004.11:g.72622566A>C , CM000666.1:g.72622566A>C	GRCh37
NC_000004.10:g.72841430A>C	NCBI36
NG_012837.2:g.53672T>G
NG_012837.3:g.53672T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000273951.13:c.897T>G MANE Select	ENSP00000273951.8:p.Cys299Trp
ENST00000273951.12:c.897T>G	ENSP00000273951.8:p.Cys299Trp
ENST00000503472.5:n.781T>G
ENST00000504199.5:c.954T>G	ENSP00000421725.1:p.Cys318Trp
ENST00000509740.5:c.897T>G	ENSP00000422664.1:p.Cys299Trp
ENST00000513476.5:c.897T>G	ENSP00000426683.1:p.Cys299Trp
NM_000583.3:c.897T>G	NP_000574.2:p.Cys299Trp
NM_001204306.1:c.897T>G	NP_001191235.1:p.Cys299Trp
NM_001204307.1:c.954T>G	NP_001191236.1:p.Cys318Trp
XM_006714177.2:c.897T>G	XP_006714240.1:p.Cys299Trp
XM_006714177.3:c.897T>G	XP_006714240.1:p.Cys299Trp
NM_000583.4:c.897T>G MANE Select	NP_000574.2:p.Cys299Trp