Canonical Allele Identifier: CA2407514228
Gene: SAMM50 HGNC NCBI

Linked Data

dbSNP Id: rs796757746

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43998433C>G , CM000684.2:g.43998433C>G GRCh38
NC_000022.10:g.44394313C>G , CM000684.1:g.44394313C>G GRCh37
NC_000022.9:g.42725646C>G NCBI36
NG_029057.1:g.48053C>G
NG_029743.1:g.4223C>G
NG_029057.2:g.48053C>G
NG_029743.2:g.4223C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000465768.1:n.79+8027C>G