Canonical Allele Identifier: CA2407514290
Gene: SAMM50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43998586C= , CM000684.2:g.43998586C= GRCh38
NC_000022.10:g.44394466C= , CM000684.1:g.44394466C= GRCh37
NC_000022.9:g.42725799C= NCBI36
NG_029743.1:g.4376C=
NG_029743.2:g.4376C=

Transcript Alleles

HGVS Amino-acid change
ENST00000465768.1:n.79+8180C=