Canonical Allele Identifier: CA2407514226
Gene: SAMM50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43998432G= , CM000684.2:g.43998432G= GRCh38
NC_000022.10:g.44394312G= , CM000684.1:g.44394312G= GRCh37
NC_000022.9:g.42725645G= NCBI36
NG_029057.1:g.48052G=
NG_029743.1:g.4222G=
NG_029057.2:g.48052G=
NG_029743.2:g.4222G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465768.1:n.79+8026G=