Canonical Allele Identifier: CA1309449454
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176127051A= , CM000664.2:g.176127051A= GRCh38
NC_000002.11:g.176991779A= , CM000664.1:g.176991779A= GRCh37
NC_000002.10:g.176700025A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_241351.3:n.2581T=