Canonical Allele Identifier: CA2407514270
Gene: SAMM50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43998527T= , CM000684.2:g.43998527T= GRCh38
NC_000022.10:g.44394407T= , CM000684.1:g.44394407T= GRCh37
NC_000022.9:g.42725740T= NCBI36
NG_029057.1:g.48147T=
NG_029743.1:g.4317T=
NG_029057.2:g.48147T=
NG_029743.2:g.4317T=

Transcript Alleles

HGVS Amino-acid change
ENST00000465768.1:n.79+8121T=