Canonical Allele Identifier: CA552292686

Gene: GC

Linked Data

• dbSNP Id: rs1488738043
• gnomAD v2: 4-72649786-G-T
• gnomAD v4: 4-71784069-G-T
• MyVariant Identifiers: chr4:g.72649786G>T (hg19) ; chr4:g.71784069G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71784069G>T , CM000666.2:g.71784069G>T	GRCh38
NC_000004.11:g.72649786G>T , CM000666.1:g.72649786G>T	GRCh37
NC_000004.10:g.72868650G>T	NCBI36
NG_012837.2:g.26452C>A
NG_012837.3:g.26452C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000273951.13:c.-51C>A MANE Select	ENSP00000273951.8:n.-51C>A
ENST00000273951.12:c.-51C>A	ENSP00000273951.8:n.-51C>A
ENST00000504199.5:c.22-15C>A	ENSP00000421725.1:n.22-15C>A
ENST00000506245.1:c.-36-15C>A	ENSP00000426718.1:n.-36-15C>A
NM_000583.3:c.-51C>A	NP_000574.2:n.-51C>A
NM_001204306.1:c.-36-15C>A	NP_001191235.1:n.-36-15C>A
NM_001204307.1:c.22-15C>A	NP_001191236.1:n.22-15C>A
XM_006714177.2:c.-51C>A	XP_006714240.1:n.-51C>A
XM_006714177.3:c.-51C>A	XP_006714240.1:n.-51C>A
NM_000583.4:c.-51C>A MANE Select	NP_000574.2:n.-51C>A