Canonical Allele Identifier: CA1207463741
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172741803T= , CM000663.2:g.172741803T= GRCh38
NC_000001.10:g.172710943T= , CM000663.1:g.172710943T= GRCh37
NC_000001.9:g.170977566T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922289.1:n.27-34016T=