Canonical Allele Identifier: CA1284436069
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122379216T= , CM000664.2:g.122379216T= GRCh38
NC_000002.11:g.123136792T= , CM000664.1:g.123136792T= GRCh37
NC_000002.10:g.122853262T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923278.1:n.556-13747T=
XR_001739684.1:n.556-13747T=