Canonical Allele Identifier: CA375578613
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136674775-G-C
MyVariant Identifiers: chr9:g.139569227G>C (hg19) chr9:g.136674775G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674775G>C , CM000671.2:g.136674775G>C GRCh38
NC_000009.11:g.139569227G>C , CM000671.1:g.139569227G>C GRCh37
NC_000009.10:g.138689048G>C NCBI36
NG_008090.1:g.17685C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.621C>G MANE Select ENSP00000360761.2:p.Phe207Leu
ENST00000371694.7:c.525C>G ENSP00000360759.3:p.Phe175Leu
ENST00000371696.6:c.621C>G ENSP00000360761.2:p.Phe207Leu
ENST00000472820.1:n.549C>G
ENST00000538402.1:c.621C>G ENSP00000438919.1:p.Phe207Leu
NM_001012727.1:c.525C>G NP_001012745.1:p.Phe175Leu
NM_006412.3:c.621C>G NP_006403.2:p.Phe207Leu
NM_006412.4:c.621C>G MANE Select NP_006403.2:p.Phe207Leu
NM_001012727.2:c.525C>G NP_001012745.1:p.Phe175Leu
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