Canonical Allele Identifier: CA861082731
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1323122484
MyVariant Identifiers: chr9:g.139571321T>C (hg19) chr9:g.136676869T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136676869T>C , CM000671.2:g.136676869T>C GRCh38
NC_000009.11:g.139571321T>C , CM000671.1:g.139571321T>C GRCh37
NC_000009.10:g.138691142T>C NCBI36
NG_008090.1:g.15591A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.492+92A>G MANE Select ENSP00000360761.2:n.492+92A>G
ENST00000371694.7:c.492+92A>G ENSP00000360759.3:n.492+92A>G
ENST00000371696.6:c.492+92A>G ENSP00000360761.2:n.492+92A>G
ENST00000472820.1:n.420+92A>G
ENST00000538402.1:c.492+92A>G ENSP00000438919.1:n.492+92A>G
NM_001012727.1:c.492+92A>G NP_001012745.1:n.492+92A>G
NM_006412.3:c.492+92A>G NP_006403.2:n.492+92A>G
NM_006412.4:c.492+92A>G MANE Select NP_006403.2:n.492+92A>G
NM_001012727.2:c.492+92A>G NP_001012745.1:n.492+92A>G
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