Canonical Allele Identifier: CA1207463786
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172741892G= , CM000663.2:g.172741892G= GRCh38
NC_000001.10:g.172711032G= , CM000663.1:g.172711032G= GRCh37
NC_000001.9:g.170977655G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922289.1:n.27-33927G=