Canonical Allele Identifier: CA1841175508
Gene:

Linked Data

dbSNP Id: rs1819675122

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551299T>A , CM000671.2:g.25551299T>A GRCh38
NC_000009.11:g.25551297T>A , CM000671.1:g.25551297T>A GRCh37
NC_000009.10:g.25541297T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929525.1:n.50-727A>T
XR_929525.2:n.674-727A>T