Canonical Allele Identifier: CA2955568

Gene: GC

Linked Data

• dbSNP Id: rs776954334
• ExAC: 4:72622661 G / C
• gnomAD v2: 4-72622661-G-C
• MyVariant Identifiers: chr4:g.72622661G>C (hg19) ; chr4:g.71756944G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71756944G>C , CM000666.2:g.71756944G>C	GRCh38
NC_000004.11:g.72622661G>C , CM000666.1:g.72622661G>C	GRCh37
NC_000004.10:g.72841525G>C	NCBI36
NG_012837.2:g.53577C>G
NG_012837.3:g.53577C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.832-30C>G MANE Select	ENSP00000273951.8:n.832-30C>G
ENST00000273951.12:c.832-30C>G	ENSP00000273951.8:n.832-30C>G
ENST00000503472.5:n.716-30C>G
ENST00000504199.5:c.889-30C>G	ENSP00000421725.1:n.889-30C>G
ENST00000509740.5:c.832-30C>G	ENSP00000422664.1:n.832-30C>G
ENST00000513476.5:c.832-30C>G	ENSP00000426683.1:n.832-30C>G
NM_000583.3:c.832-30C>G	NP_000574.2:n.832-30C>G
NM_001204306.1:c.832-30C>G	NP_001191235.1:n.832-30C>G
NM_001204307.1:c.889-30C>G	NP_001191236.1:n.889-30C>G
XM_006714177.2:c.832-30C>G	XP_006714240.1:n.832-30C>G
XM_006714177.3:c.832-30C>G	XP_006714240.1:n.832-30C>G
NM_000583.4:c.832-30C>G MANE Select	NP_000574.2:n.832-30C>G