Canonical Allele Identifier: CA2407514248
Gene: SAMM50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43998464A= , CM000684.2:g.43998464A= GRCh38
NC_000022.10:g.44394344A= , CM000684.1:g.44394344A= GRCh37
NC_000022.9:g.42725677A= NCBI36
NG_029057.1:g.48084A=
NG_029743.1:g.4254A=
NG_029057.2:g.48084A=
NG_029743.2:g.4254A=

Transcript Alleles

HGVS Amino-acid change
ENST00000465768.1:n.79+8058A=