Canonical Allele Identifier: CA1284431665
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122368888A= , CM000664.2:g.122368888A= GRCh38
NC_000002.11:g.123126464A= , CM000664.1:g.123126464A= GRCh37
NC_000002.10:g.122842934A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923278.1:n.556-24075A=
XR_001739684.1:n.556-24075A=