Canonical Allele Identifier: CA99074834

Gene: GC

Linked Data

• dbSNP Id: rs981176637
• MyVariant Identifiers: chr4:g.72650887G>A (hg19) ; chr4:g.71785170G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71785170G>A , CM000666.2:g.71785170G>A	GRCh38
NC_000004.11:g.72650887G>A , CM000666.1:g.72650887G>A	GRCh37
NC_000004.10:g.72869751G>A	NCBI36
NG_012837.2:g.25351C>T
NG_012837.3:g.25351C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000504199.5:c.22-1116C>T	ENSP00000421725.1:n.22-1116C>T
ENST00000506245.1:c.-37+750C>T	ENSP00000426718.1:n.-37+750C>T
NM_001204306.1:c.-36-1116C>T	NP_001191235.1:n.-36-1116C>T
NM_001204307.1:c.22-1116C>T	NP_001191236.1:n.22-1116C>T