Canonical Allele Identifier: CA375580868
Gene: AGPAT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.139571057A>T (hg19) chr9:g.136676605A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136676605A>T , CM000671.2:g.136676605A>T GRCh38
NC_000009.11:g.139571057A>T , CM000671.1:g.139571057A>T GRCh37
NC_000009.10:g.138690878A>T NCBI36
NG_008090.1:g.15855T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.568T>A MANE Select ENSP00000360761.2:p.Tyr190Asn
ENST00000371694.7:c.492+356T>A ENSP00000360759.3:n.492+356T>A
ENST00000371696.6:c.568T>A ENSP00000360761.2:p.Tyr190Asn
ENST00000472820.1:n.496T>A
ENST00000538402.1:c.568T>A ENSP00000438919.1:p.Tyr190Asn
NM_001012727.1:c.492+356T>A NP_001012745.1:n.492+356T>A
NM_006412.3:c.568T>A NP_006403.2:p.Tyr190Asn
NM_006412.4:c.568T>A MANE Select NP_006403.2:p.Tyr190Asn
NM_001012727.2:c.492+356T>A NP_001012745.1:n.492+356T>A
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