Canonical Allele Identifier: CA5342994
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs374919945
ExAC: 9:139571429 C / T
gnomAD v2: 9-139571429-C-T
gnomAD v3: 9-136676977-C-T
gnomAD v4: 9-136676977-C-T
MyVariant Identifiers: chr9:g.139571429C>T (hg19) chr9:g.136676977C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136676977C>T , CM000671.2:g.136676977C>T GRCh38
NC_000009.11:g.139571429C>T , CM000671.1:g.139571429C>T GRCh37
NC_000009.10:g.138691250C>T NCBI36
NG_008090.1:g.15483G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.476G>A MANE Select ENSP00000360761.2:p.Arg159His
ENST00000371694.7:c.476G>A ENSP00000360759.3:p.Arg159His
ENST00000371696.6:c.476G>A ENSP00000360761.2:p.Arg159His
ENST00000472820.1:n.404G>A
ENST00000538402.1:c.476G>A ENSP00000438919.1:p.Arg159His
NM_001012727.1:c.476G>A NP_001012745.1:p.Arg159His
NM_006412.3:c.476G>A NP_006403.2:p.Arg159His
NM_006412.4:c.476G>A MANE Select NP_006403.2:p.Arg159His
NM_001012727.2:c.476G>A NP_001012745.1:p.Arg159His
Search 100 bp 5'
Search 100 bp 3'