Canonical Allele Identifier: CA375577625
Gene: AGPAT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.139568347G>T (hg19) chr9:g.136673895G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673895G>T , CM000671.2:g.136673895G>T GRCh38
NC_000009.11:g.139568347G>T , CM000671.1:g.139568347G>T GRCh37
NC_000009.10:g.138688168G>T NCBI36
NG_008090.1:g.18565C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.694C>A MANE Select ENSP00000360761.2:p.Pro232Thr
ENST00000371694.7:c.598C>A ENSP00000360759.3:p.Pro200Thr
ENST00000371696.6:c.694C>A ENSP00000360761.2:p.Pro232Thr
ENST00000472820.1:n.622C>A
ENST00000538402.1:c.694C>A ENSP00000438919.1:p.Pro232Thr
NM_001012727.1:c.598C>A NP_001012745.1:p.Pro200Thr
NM_006412.3:c.694C>A NP_006403.2:p.Pro232Thr
NM_006412.4:c.694C>A MANE Select NP_006403.2:p.Pro232Thr
NM_001012727.2:c.598C>A NP_001012745.1:p.Pro200Thr
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