Canonical Allele Identifier: CA2407514230
Gene: SAMM50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43998441T= , CM000684.2:g.43998441T= GRCh38
NC_000022.10:g.44394321T= , CM000684.1:g.44394321T= GRCh37
NC_000022.9:g.42725654T= NCBI36
NG_029057.1:g.48061T=
NG_029743.1:g.4231T=
NG_029057.2:g.48061T=
NG_029743.2:g.4231T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465768.1:n.79+8035T=