Canonical Allele Identifier: CA1326220242
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.212959321A= , CM000664.2:g.212959321A= GRCh38
NC_000002.11:g.213824045A= , CM000664.1:g.213824045A= GRCh37
NC_000002.10:g.213532290A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739869.1:n.2124+6063T=
XR_923849.1:n.484+6063T=