Canonical Allele Identifier: CA2381739141
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.22259291T= , CM000683.2:g.22259291T= GRCh38
NC_000021.8:g.23631611T= , CM000683.1:g.23631611T= GRCh37
NC_000021.7:g.22553482T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754978.1:n.221+46478T=