Canonical Allele Identifier: CA357204896

Gene: GC

Linked Data

• dbSNP Id: rs762123144
• gnomAD v3: 4-71756835-G-C
• gnomAD v4: 4-71756835-G-C
• MyVariant Identifiers: chr4:g.72622552G>C (hg19) ; chr4:g.71756835G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71756835G>C , CM000666.2:g.71756835G>C	GRCh38
NC_000004.11:g.72622552G>C , CM000666.1:g.72622552G>C	GRCh37
NC_000004.10:g.72841416G>C	NCBI36
NG_012837.2:g.53686C>G
NG_012837.3:g.53686C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.911C>G MANE Select	ENSP00000273951.8:p.Thr304Arg
ENST00000273951.12:c.911C>G	ENSP00000273951.8:p.Thr304Arg
ENST00000503472.5:n.795C>G
ENST00000504199.5:c.968C>G	ENSP00000421725.1:p.Thr323Arg
ENST00000509740.5:c.911C>G	ENSP00000422664.1:p.Thr304Arg
ENST00000513476.5:c.911C>G	ENSP00000426683.1:p.Thr304Arg
NM_000583.3:c.911C>G	NP_000574.2:p.Thr304Arg
NM_001204306.1:c.911C>G	NP_001191235.1:p.Thr304Arg
NM_001204307.1:c.968C>G	NP_001191236.1:p.Thr323Arg
XM_006714177.2:c.911C>G	XP_006714240.1:p.Thr304Arg
XM_006714177.3:c.911C>G	XP_006714240.1:p.Thr304Arg
NM_000583.4:c.911C>G MANE Select	NP_000574.2:p.Thr304Arg