Canonical Allele Identifier: CA99074795

Gene: GC

Linked Data

• dbSNP Id: rs183396402
• gnomAD v2: 4-72650627-T-C
• gnomAD v3: 4-71784910-T-C
• gnomAD v4: 4-71784910-T-C
• MyVariant Identifiers: chr4:g.72650627T>C (hg19) ; chr4:g.71784910T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71784910T>C , CM000666.2:g.71784910T>C	GRCh38
NC_000004.11:g.72650627T>C , CM000666.1:g.72650627T>C	GRCh37
NC_000004.10:g.72869491T>C	NCBI36
NG_012837.2:g.25611A>G
NG_012837.3:g.25611A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000504199.5:c.22-856A>G	ENSP00000421725.1:n.22-856A>G
ENST00000506245.1:c.-36-856A>G	ENSP00000426718.1:n.-36-856A>G
NM_001204306.1:c.-36-856A>G	NP_001191235.1:n.-36-856A>G
NM_001204307.1:c.22-856A>G	NP_001191236.1:n.22-856A>G