Canonical Allele Identifier: CA375580920
Gene: AGPAT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.139571066C>G (hg19) chr9:g.136676614C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136676614C>G , CM000671.2:g.136676614C>G GRCh38
NC_000009.11:g.139571066C>G , CM000671.1:g.139571066C>G GRCh37
NC_000009.10:g.138690887C>G NCBI36
NG_008090.1:g.15846G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.559G>C MANE Select ENSP00000360761.2:p.Gly187Arg
ENST00000371694.7:c.492+347G>C ENSP00000360759.3:n.492+347G>C
ENST00000371696.6:c.559G>C ENSP00000360761.2:p.Gly187Arg
ENST00000472820.1:n.487G>C
ENST00000538402.1:c.559G>C ENSP00000438919.1:p.Gly187Arg
NM_001012727.1:c.492+347G>C NP_001012745.1:n.492+347G>C
NM_006412.3:c.559G>C NP_006403.2:p.Gly187Arg
NM_006412.4:c.559G>C MANE Select NP_006403.2:p.Gly187Arg
NM_001012727.2:c.492+347G>C NP_001012745.1:n.492+347G>C
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