Canonical Allele Identifier: CA2361532987
Community Standard Title: NC_000020.11:g.35165459T=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35165459T= , CM000682.2:g.35165459T= GRCh38
NC_000020.10:g.33753262T= , CM000682.1:g.33753262T= GRCh37
NC_000020.9:g.33216923T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001355008.1:c.-17+328A= NP_001341937.1:n.-17+328A=
NM_001355008.2:c.-17+328A= NP_001341937.1:n.-17+328A=