Canonical Allele Identifier: CA2407514237
Gene: SAMM50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43998448C= , CM000684.2:g.43998448C= GRCh38
NC_000022.10:g.44394328C= , CM000684.1:g.44394328C= GRCh37
NC_000022.9:g.42725661C= NCBI36
NG_029057.1:g.48068C=
NG_029743.1:g.4238C=
NG_029057.2:g.48068C=
NG_029743.2:g.4238C=

Transcript Alleles

HGVS Amino-acid change
ENST00000465768.1:n.79+8042C=