Canonical Allele Identifier: CA201623469
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs201868056
MyVariant Identifiers: chr9:g.139568181G>T (hg19) chr9:g.136673729G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673729G>T , CM000671.2:g.136673729G>T GRCh38
NC_000009.11:g.139568181G>T , CM000671.1:g.139568181G>T GRCh37
NC_000009.10:g.138688002G>T NCBI36
NG_008090.1:g.18731C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.*23C>A MANE Select ENSP00000360761.2:n.*23C>A
ENST00000371694.7:c.*23C>A ENSP00000360759.3:n.*23C>A
ENST00000371696.6:c.*23C>A ENSP00000360761.2:n.*23C>A
ENST00000472820.1:n.788C>A
ENST00000538402.1:c.*23C>A ENSP00000438919.1:n.*23C>A
NM_001012727.1:c.*23C>A NP_001012745.1:n.*23C>A
NM_006412.3:c.*23C>A NP_006403.2:n.*23C>A
NM_006412.4:c.*23C>A MANE Select NP_006403.2:n.*23C>A
NM_001012727.2:c.*23C>A NP_001012745.1:n.*23C>A
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