Canonical Allele Identifier: CA1207463782
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172741887G= , CM000663.2:g.172741887G= GRCh38
NC_000001.10:g.172711027G= , CM000663.1:g.172711027G= GRCh37
NC_000001.9:g.170977650G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922289.1:n.27-33932G=