Canonical Allele Identifier: CA155899192

Gene:

Linked Data

• dbSNP Id: rs116488206
• gnomAD v2: 7-25871058-T-C
• gnomAD v3: 7-25831438-T-C
• gnomAD v4: 7-25831438-T-C
• MyVariant Identifiers: chr7:g.25871058T>C (hg19) ; chr7:g.25831438T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.25831438T>C , CM000669.2:g.25831438T>C	GRCh38
NC_000007.13:g.25871058T>C , CM000669.1:g.25871058T>C	GRCh37
NC_000007.12:g.25837583T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_108752.3:n.469A>G
XR_927108.1:n.443A>G
XR_927109.1:n.525A>G
XR_927110.1:n.429A>G
XR_108752.4:n.483A>G
XR_927110.2:n.608A>G