Canonical Allele Identifier: CA1207463781
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172741885A= , CM000663.2:g.172741885A= GRCh38
NC_000001.10:g.172711025A= , CM000663.1:g.172711025A= GRCh37
NC_000001.9:g.170977648A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922289.1:n.27-33934A=