Canonical Allele Identifier: CA5343197
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs752498632
ExAC: 9:139581819 C / T
gnomAD v2: 9-139581819-C-T
gnomAD v3: 9-136687367-C-T
gnomAD v4: 9-136687367-C-T
MyVariant Identifiers: chr9:g.139581819C>T (hg19) chr9:g.136687367C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687367C>T , CM000671.2:g.136687367C>T GRCh38
NC_000009.11:g.139581819C>T , CM000671.1:g.139581819C>T GRCh37
NC_000009.10:g.138701640C>T NCBI36
NG_008090.1:g.5093G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.-10G>A MANE Select ENSP00000360761.2:n.-10G>A
ENST00000371694.7:c.-10G>A ENSP00000360759.3:n.-10G>A
ENST00000371696.6:c.-10G>A ENSP00000360761.2:n.-10G>A
ENST00000538402.1:c.-10G>A ENSP00000438919.1:n.-10G>A
NM_001012727.1:c.-10G>A NP_001012745.1:n.-10G>A
NM_006412.3:c.-10G>A NP_006403.2:n.-10G>A
NM_006412.4:c.-10G>A MANE Select NP_006403.2:n.-10G>A
NM_001012727.2:c.-10G>A NP_001012745.1:n.-10G>A
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