Canonical Allele Identifier: CA1215982346
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192800613T= , CM000663.2:g.192800613T= GRCh38
NC_000001.10:g.192769743T= , CM000663.1:g.192769743T= GRCh37
NC_000001.9:g.191036366T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429211.2:n.43T=