Canonical Allele Identifier: CA1889344561
Gene:

Linked Data

dbSNP Id: rs1652632019

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8697658A>G , CM000672.2:g.8697658A>G GRCh38
NC_000010.10:g.8739621A>G , CM000672.1:g.8739621A>G GRCh37
NC_000010.9:g.8779627A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930641.1:n.33-27857T>C