Canonical Allele Identifier: CA2407514279
Gene: SAMM50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43998555A= , CM000684.2:g.43998555A= GRCh38
NC_000022.10:g.44394435A= , CM000684.1:g.44394435A= GRCh37
NC_000022.9:g.42725768A= NCBI36
NG_029743.1:g.4345A=
NG_029743.2:g.4345A=

Transcript Alleles

HGVS Amino-acid change
ENST00000465768.1:n.79+8149A=