Canonical Allele Identifier: CA2720852200
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1846086683
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136676107G>A , CM000671.2:g.136676107G>A GRCh38
NC_000009.11:g.139570559G>A , CM000671.1:g.139570559G>A GRCh37
NC_000009.10:g.138690380G>A NCBI36
NG_008090.1:g.16353C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.588+478C>T MANE Select ENSP00000360761.2:n.588+478C>T
ENST00000371694.7:c.492+854C>T ENSP00000360759.3:n.492+854C>T
ENST00000371696.6:c.588+478C>T ENSP00000360761.2:n.588+478C>T
ENST00000472820.1:n.516+478C>T
ENST00000538402.1:c.588+478C>T ENSP00000438919.1:n.588+478C>T
NM_001012727.1:c.492+854C>T NP_001012745.1:n.492+854C>T
NM_006412.3:c.588+478C>T NP_006403.2:n.588+478C>T
NM_006412.4:c.588+478C>T MANE Select NP_006403.2:n.588+478C>T
NM_001012727.2:c.492+854C>T NP_001012745.1:n.492+854C>T
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