Canonical Allele Identifier: CA1889344461
Gene:

Linked Data

dbSNP Id: rs1832129558

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8697444A>G , CM000672.2:g.8697444A>G GRCh38
NC_000010.10:g.8739407A>G , CM000672.1:g.8739407A>G GRCh37
NC_000010.9:g.8779413A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930641.1:n.33-27643T>C