Canonical Allele Identifier: CA2580610013
Gene: SAMM50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43998522C>G , CM000684.2:g.43998522C>G GRCh38
NC_000022.10:g.44394402C>G , CM000684.1:g.44394402C>G GRCh37
NC_000022.9:g.42725735C>G NCBI36
NG_029057.1:g.48142C>G
NG_029743.1:g.4312C>G
NG_029057.2:g.48142C>G
NG_029743.2:g.4312C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000465768.1:n.79+8116C>G