Canonical Allele Identifier: CA1207463719
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172741762G= , CM000663.2:g.172741762G= GRCh38
NC_000001.10:g.172710902G= , CM000663.1:g.172710902G= GRCh37
NC_000001.9:g.170977525G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922289.1:n.27-34057G=