Canonical Allele Identifier: CA375577520
Gene: AGPAT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.139568331G>T (hg19) chr9:g.136673879G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673879G>T , CM000671.2:g.136673879G>T GRCh38
NC_000009.11:g.139568331G>T , CM000671.1:g.139568331G>T GRCh37
NC_000009.10:g.138688152G>T NCBI36
NG_008090.1:g.18581C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.710C>A MANE Select ENSP00000360761.2:p.Thr237Asn
ENST00000371694.7:c.614C>A ENSP00000360759.3:p.Thr205Asn
ENST00000371696.6:c.710C>A ENSP00000360761.2:p.Thr237Asn
ENST00000472820.1:n.638C>A
ENST00000538402.1:c.710C>A ENSP00000438919.1:p.Thr237Asn
NM_001012727.1:c.614C>A NP_001012745.1:p.Thr205Asn
NM_006412.3:c.710C>A NP_006403.2:p.Thr237Asn
NM_006412.4:c.710C>A MANE Select NP_006403.2:p.Thr237Asn
NM_001012727.2:c.614C>A NP_001012745.1:p.Thr205Asn
Search 100 bp 5'
Search 100 bp 3'