Canonical Allele Identifier: CA439799364

Gene: GC

Linked Data

• gnomAD v4: 4-71783962-T-C
• MyVariant Identifiers: chr4:g.72649679T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71783962T>C , CM000666.2:g.71783962T>C	GRCh38
NC_000004.11:g.72649679T>C , CM000666.1:g.72649679T>C	GRCh37
NC_000004.10:g.72868543T>C	NCBI36
NG_012837.2:g.26559A>G
NG_012837.3:g.26559A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000273951.13:c.57A>G MANE Select	ENSP00000273951.8:p.Arg19=
ENST00000273951.12:c.57A>G	ENSP00000273951.8:p.Arg19=
ENST00000504199.5:c.114A>G	ENSP00000421725.1:p.Arg38=
ENST00000506245.1:c.57A>G	ENSP00000426718.1:p.Arg19=
ENST00000509740.5:c.57A>G	ENSP00000422664.1:p.Arg19=
ENST00000513476.5:c.57A>G	ENSP00000426683.1:p.Arg19=
NM_000583.3:c.57A>G	NP_000574.2:p.Arg19=
NM_001204306.1:c.57A>G	NP_001191235.1:p.Arg19=
NM_001204307.1:c.114A>G	NP_001191236.1:p.Arg38=
XM_006714177.2:c.57A>G	XP_006714240.1:p.Arg19=
XM_006714177.3:c.57A>G	XP_006714240.1:p.Arg19=
NM_000583.4:c.57A>G MANE Select	NP_000574.2:p.Arg19=