Canonical Allele Identifier: CA456626294
Gene: SAMD9 HGNC NCBI

Linked Data

dbSNP Id: rs1321909248
gnomAD v2: 7-92733356-T-G
gnomAD v3: 7-93104043-T-G
gnomAD v4: 7-93104043-T-G
MyVariant Identifiers: chr7:g.92733356T>G (hg19) chr7:g.93104043T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93104043T>G , CM000669.2:g.93104043T>G GRCh38
NC_000007.13:g.92733356T>G , CM000669.1:g.92733356T>G GRCh37
NC_000007.12:g.92571292T>G NCBI36
NG_023419.1:g.18981A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000379958.3:c.2055A>C MANE Select ENSP00000369292.2:p.Arg685=
ENST00000379958.2:c.2055A>C ENSP00000369292.2:p.Arg685=
ENST00000446617.1:c.2055A>C ENSP00000414529.1:p.Arg685=
ENST00000620985.4:c.2055A>C ENSP00000484636.1:p.Arg685=
NM_001193307.1:c.2055A>C NP_001180236.1:p.Arg685=
NM_017654.3:c.2055A>C NP_060124.2:p.Arg685=
NM_017654.4:c.2055A>C MANE Select NP_060124.2:p.Arg685=
NM_001193307.2:c.2055A>C NP_001180236.1:p.Arg685=
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