Canonical Allele Identifier: CA201628808
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1015212091
MyVariant Identifiers: chr9:g.139570597C>G (hg19) chr9:g.136676145C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136676145C>G , CM000671.2:g.136676145C>G GRCh38
NC_000009.11:g.139570597C>G , CM000671.1:g.139570597C>G GRCh37
NC_000009.10:g.138690418C>G NCBI36
NG_008090.1:g.16315G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.588+440G>C MANE Select ENSP00000360761.2:n.588+440G>C
ENST00000371694.7:c.492+816G>C ENSP00000360759.3:n.492+816G>C
ENST00000371696.6:c.588+440G>C ENSP00000360761.2:n.588+440G>C
ENST00000472820.1:n.516+440G>C
ENST00000538402.1:c.588+440G>C ENSP00000438919.1:n.588+440G>C
NM_001012727.1:c.492+816G>C NP_001012745.1:n.492+816G>C
NM_006412.3:c.588+440G>C NP_006403.2:n.588+440G>C
NM_006412.4:c.588+440G>C MANE Select NP_006403.2:n.588+440G>C
NM_001012727.2:c.492+816G>C NP_001012745.1:n.492+816G>C
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