Canonical Allele Identifier: CA1889344567
Gene:

Linked Data

dbSNP Id: rs1832130862

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8697679A>T , CM000672.2:g.8697679A>T GRCh38
NC_000010.10:g.8739642A>T , CM000672.1:g.8739642A>T GRCh37
NC_000010.9:g.8779648A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930641.1:n.33-27878T>A