Canonical Allele Identifier: CA467738759
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136676618-C-T
MyVariant Identifiers: chr9:g.139571070C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136676618C>T , CM000671.2:g.136676618C>T GRCh38
NC_000009.11:g.139571070C>T , CM000671.1:g.139571070C>T GRCh37
NC_000009.10:g.138690891C>T NCBI36
NG_008090.1:g.15842G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.555G>A MANE Select ENSP00000360761.2:p.Lys185=
ENST00000371694.7:c.492+343G>A ENSP00000360759.3:n.492+343G>A
ENST00000371696.6:c.555G>A ENSP00000360761.2:p.Lys185=
ENST00000472820.1:n.483G>A
ENST00000538402.1:c.555G>A ENSP00000438919.1:p.Lys185=
NM_001012727.1:c.492+343G>A NP_001012745.1:n.492+343G>A
NM_006412.3:c.555G>A NP_006403.2:p.Lys185=
NM_006412.4:c.555G>A MANE Select NP_006403.2:p.Lys185=
NM_001012727.2:c.492+343G>A NP_001012745.1:n.492+343G>A
Search 100 bp 5'
Search 100 bp 3'