Canonical Allele Identifier: CA1300434477
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.156270452T= , CM000664.2:g.156270452T= GRCh38
NC_000002.11:g.157126964T= , CM000664.1:g.157126964T= GRCh37
NC_000002.10:g.156835210T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923502.1:n.1303-42448A=