Canonical Allele Identifier: CA2407514272
Gene: SAMM50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43998533G= , CM000684.2:g.43998533G= GRCh38
NC_000022.10:g.44394413G= , CM000684.1:g.44394413G= GRCh37
NC_000022.9:g.42725746G= NCBI36
NG_029743.1:g.4323G=
NG_029743.2:g.4323G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465768.1:n.79+8127G=