Canonical Allele Identifier: CA2407514287
Gene: SAMM50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43998575C= , CM000684.2:g.43998575C= GRCh38
NC_000022.10:g.44394455C= , CM000684.1:g.44394455C= GRCh37
NC_000022.9:g.42725788C= NCBI36
NG_029743.1:g.4365C=
NG_029743.2:g.4365C=

Transcript Alleles

HGVS Amino-acid change
ENST00000465768.1:n.79+8169C=