Canonical Allele Identifier: CA2738206768
Gene: SAMM50 HGNC NCBI

Linked Data

dbSNP Id: rs2146835824

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43998454A>G , CM000684.2:g.43998454A>G GRCh38
NC_000022.10:g.44394334A>G , CM000684.1:g.44394334A>G GRCh37
NC_000022.9:g.42725667A>G NCBI36
NG_029057.1:g.48074A>G
NG_029743.1:g.4244A>G
NG_029057.2:g.48074A>G
NG_029743.2:g.4244A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000465768.1:n.79+8048A>G