Canonical Allele Identifier: CA456626306
Gene: SAMD9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1956647
ClinVar RCV Id: RCV002701000
dbSNP Id: rs1223114982
gnomAD v2: 7-92733371-C-T
gnomAD v3: 7-93104058-C-T
gnomAD v4: 7-93104058-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93104058C>T , CM000669.2:g.93104058C>T GRCh38
NC_000007.13:g.92733371C>T , CM000669.1:g.92733371C>T GRCh37
NC_000007.12:g.92571307C>T NCBI36
NG_023419.1:g.18966G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000379958.3:c.2040G>A MANE Select ENSP00000369292.2:p.Glu680=
ENST00000379958.2:c.2040G>A ENSP00000369292.2:p.Glu680=
ENST00000446617.1:c.2040G>A ENSP00000414529.1:p.Glu680=
ENST00000620985.4:c.2040G>A ENSP00000484636.1:p.Glu680=
NM_001193307.1:c.2040G>A NP_001180236.1:p.Glu680=
NM_017654.3:c.2040G>A NP_060124.2:p.Glu680=
NM_017654.4:c.2040G>A MANE Select NP_060124.2:p.Glu680=
NM_001193307.2:c.2040G>A NP_001180236.1:p.Glu680=