Canonical Allele Identifier: CA1130035191

Gene: AGPAT2

Linked Data

• dbSNP Id: rs1846086573
• gnomAD v3: 9-136676101-G-C
• gnomAD v4: 9-136676101-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676101G>C , CM000671.2:g.136676101G>C	GRCh38
NC_000009.11:g.139570553G>C , CM000671.1:g.139570553G>C	GRCh37
NC_000009.10:g.138690374G>C	NCBI36
NG_008090.1:g.16359C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371696.7:c.588+484C>G MANE Select	ENSP00000360761.2:n.588+484C>G
ENST00000371694.7:c.492+860C>G	ENSP00000360759.3:n.492+860C>G
ENST00000371696.6:c.588+484C>G	ENSP00000360761.2:n.588+484C>G
ENST00000472820.1:n.516+484C>G
ENST00000538402.1:c.588+484C>G	ENSP00000438919.1:n.588+484C>G
NM_001012727.1:c.492+860C>G	NP_001012745.1:n.492+860C>G
NM_006412.3:c.588+484C>G	NP_006403.2:n.588+484C>G
NM_006412.4:c.588+484C>G MANE Select	NP_006403.2:n.588+484C>G
NM_001012727.2:c.492+860C>G	NP_001012745.1:n.492+860C>G