Canonical Allele Identifier: CA1329960821
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.221034724C= , CM000664.2:g.221034724C= GRCh38
NC_000002.11:g.221899444C= , CM000664.1:g.221899444C= GRCh37
NC_000002.10:g.221607688C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739897.1:n.187+1546G=