Canonical Allele Identifier: CA456626168

Gene: SAMD9

Linked Data

• MyVariant Identifiers: chr7:g.92733125C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93103812C>G , CM000669.2:g.93103812C>G	GRCh38
NC_000007.13:g.92733125C>G , CM000669.1:g.92733125C>G	GRCh37
NC_000007.12:g.92571061C>G	NCBI36
NG_023419.1:g.19212G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379958.3:c.2286G>C MANE Select	ENSP00000369292.2:p.Val762=
ENST00000379958.2:c.2286G>C	ENSP00000369292.2:p.Val762=
ENST00000446617.1:c.2286G>C	ENSP00000414529.1:p.Val762=
ENST00000620985.4:c.2286G>C	ENSP00000484636.1:p.Val762=
NM_001193307.1:c.2286G>C	NP_001180236.1:p.Val762=
NM_017654.3:c.2286G>C	NP_060124.2:p.Val762=
NM_017654.4:c.2286G>C MANE Select	NP_060124.2:p.Val762=
NM_001193307.2:c.2286G>C	NP_001180236.1:p.Val762=