Canonical Allele Identifier: CA2407514242
Gene: SAMM50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43998459A= , CM000684.2:g.43998459A= GRCh38
NC_000022.10:g.44394339A= , CM000684.1:g.44394339A= GRCh37
NC_000022.9:g.42725672A= NCBI36
NG_029057.1:g.48079A=
NG_029743.1:g.4249A=
NG_029057.2:g.48079A=
NG_029743.2:g.4249A=

Transcript Alleles

HGVS Amino-acid change
ENST00000465768.1:n.79+8053A=