Canonical Allele Identifier: CA375577222
Gene: AGPAT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.139568269G>C (hg19) chr9:g.136673817G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673817G>C , CM000671.2:g.136673817G>C GRCh38
NC_000009.11:g.139568269G>C , CM000671.1:g.139568269G>C GRCh37
NC_000009.10:g.138688090G>C NCBI36
NG_008090.1:g.18643C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.772C>G MANE Select ENSP00000360761.2:p.His258Asp
ENST00000371694.7:c.676C>G ENSP00000360759.3:p.His226Asp
ENST00000371696.6:c.772C>G ENSP00000360761.2:p.His258Asp
ENST00000472820.1:n.700C>G
ENST00000538402.1:c.772C>G ENSP00000438919.1:p.His258Asp
NM_001012727.1:c.676C>G NP_001012745.1:p.His226Asp
NM_006412.3:c.772C>G NP_006403.2:p.His258Asp
NM_006412.4:c.772C>G MANE Select NP_006403.2:p.His258Asp
NM_001012727.2:c.676C>G NP_001012745.1:p.His226Asp
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