Canonical Allele Identifier: CA324877596
Gene: SAMM50 HGNC NCBI

Linked Data

dbSNP Id: rs567335084
gnomAD v3: 22-43998431-C-G
gnomAD v4: 22-43998431-C-G
MyVariant Identifiers: chr22:g.44394311C>G (hg19) chr22:g.43998431C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43998431C>G , CM000684.2:g.43998431C>G GRCh38
NC_000022.10:g.44394311C>G , CM000684.1:g.44394311C>G GRCh37
NC_000022.9:g.42725644C>G NCBI36
NG_029057.1:g.48051C>G
NG_029743.1:g.4221C>G
NG_029057.2:g.48051C>G
NG_029743.2:g.4221C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000465768.1:n.79+8025C>G
Search 100 bp 5'
Search 100 bp 3'