Canonical Allele Identifier: CA860367834
Gene:

Linked Data

dbSNP Id: rs1319077630

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129576734G>A , CM000671.2:g.129576734G>A GRCh38
NC_000009.11:g.132339013G>A , CM000671.1:g.132339013G>A GRCh37
NC_000009.10:g.131378834G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930390.1:n.182+1136G>A