Canonical Allele Identifier: CA891092044
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171122735A>T , CM000663.2:g.171122735A>T GRCh38
NC_000001.10:g.171091875A>T , CM000663.1:g.171091875A>T GRCh37
NC_000001.9:g.169358499A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922278.1:n.593-872T>A
XR_001738291.2:n.1392-872T>A
XR_922278.3:n.1392-872T>A