Canonical Allele Identifier: CA2407514222
Gene: SAMM50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43998423G= , CM000684.2:g.43998423G= GRCh38
NC_000022.10:g.44394303G= , CM000684.1:g.44394303G= GRCh37
NC_000022.9:g.42725636G= NCBI36
NG_029057.1:g.48043G=
NG_029743.1:g.4213G=
NG_029057.2:g.48043G=
NG_029743.2:g.4213G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465768.1:n.79+8017G=