Canonical Allele Identifier: CA99487276

Gene: GC

Linked Data

• dbSNP Id: rs948702249
• gnomAD v3: 4-71790615-A-G
• gnomAD v4: 4-71790615-A-G
• MyVariant Identifiers: chr4:g.72656332A>G (hg19) ; chr4:g.71790615A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71790615A>G , CM000666.2:g.71790615A>G	GRCh38
NC_000004.11:g.72656332A>G , CM000666.1:g.72656332A>G	GRCh37
NC_000004.10:g.72875196A>G	NCBI36
NG_012837.2:g.19906T>C
NG_012837.3:g.19906T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000504199.5:c.22-6561T>C	ENSP00000421725.1:n.22-6561T>C
NM_001204306.1:c.-36-6561T>C	NP_001191235.1:n.-36-6561T>C
NM_001204307.1:c.22-6561T>C	NP_001191236.1:n.22-6561T>C