Canonical Allele Identifier: CA467737018
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136673848-G-T
MyVariant Identifiers: chr9:g.139568300G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673848G>T , CM000671.2:g.136673848G>T GRCh38
NC_000009.11:g.139568300G>T , CM000671.1:g.139568300G>T GRCh37
NC_000009.10:g.138688121G>T NCBI36
NG_008090.1:g.18612C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.741C>A MANE Select ENSP00000360761.2:p.Thr247=
ENST00000371694.7:c.645C>A ENSP00000360759.3:p.Thr215=
ENST00000371696.6:c.741C>A ENSP00000360761.2:p.Thr247=
ENST00000472820.1:n.669C>A
ENST00000538402.1:c.741C>A ENSP00000438919.1:p.Thr247=
NM_001012727.1:c.645C>A NP_001012745.1:p.Thr215=
NM_006412.3:c.741C>A NP_006403.2:p.Thr247=
NM_006412.4:c.741C>A MANE Select NP_006403.2:p.Thr247=
NM_001012727.2:c.645C>A NP_001012745.1:p.Thr215=
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