Canonical Allele Identifier: CA456626228

Gene: SAMD9

Linked Data

• gnomAD v4: 7-93103980-G-T
• MyVariant Identifiers: chr7:g.92733293G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93103980G>T , CM000669.2:g.93103980G>T	GRCh38
NC_000007.13:g.92733293G>T , CM000669.1:g.92733293G>T	GRCh37
NC_000007.12:g.92571229G>T	NCBI36
NG_023419.1:g.19044C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379958.3:c.2118C>A MANE Select	ENSP00000369292.2:p.Val706=
ENST00000379958.2:c.2118C>A	ENSP00000369292.2:p.Val706=
ENST00000446617.1:c.2118C>A	ENSP00000414529.1:p.Val706=
ENST00000620985.4:c.2118C>A	ENSP00000484636.1:p.Val706=
NM_001193307.1:c.2118C>A	NP_001180236.1:p.Val706=
NM_017654.3:c.2118C>A	NP_060124.2:p.Val706=
NM_017654.4:c.2118C>A MANE Select	NP_060124.2:p.Val706=
NM_001193307.2:c.2118C>A	NP_001180236.1:p.Val706=