Canonical Allele Identifier: CA2407514269
Gene: SAMM50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43998524G= , CM000684.2:g.43998524G= GRCh38
NC_000022.10:g.44394404G= , CM000684.1:g.44394404G= GRCh37
NC_000022.9:g.42725737G= NCBI36
NG_029057.1:g.48144G=
NG_029743.1:g.4314G=
NG_029057.2:g.48144G=
NG_029743.2:g.4314G=

Transcript Alleles

HGVS Amino-acid change
ENST00000465768.1:n.79+8118G=