Canonical Allele Identifier: CA201641276

Gene: AGPAT2

Linked Data

• dbSNP Id: rs939309307
• gnomAD v2: 9-139581552-G-A
• gnomAD v3: 9-136687100-G-A
• gnomAD v4: 9-136687100-G-A
• MyVariant Identifiers: chr9:g.139581552G>A (hg19) ; chr9:g.136687100G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687100G>A , CM000671.2:g.136687100G>A	GRCh38
NC_000009.11:g.139581552G>A , CM000671.1:g.139581552G>A	GRCh37
NC_000009.10:g.138701373G>A	NCBI36
NG_008090.1:g.5360C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.182+76C>T MANE Select	ENSP00000360761.2:n.182+76C>T
ENST00000371694.7:c.182+76C>T	ENSP00000360759.3:n.182+76C>T
ENST00000371696.6:c.182+76C>T	ENSP00000360761.2:n.182+76C>T
ENST00000470861.1:n.190+76C>T
ENST00000538402.1:c.182+76C>T	ENSP00000438919.1:n.182+76C>T
NM_001012727.1:c.182+76C>T	NP_001012745.1:n.182+76C>T
NM_006412.3:c.182+76C>T	NP_006403.2:n.182+76C>T
NM_006412.4:c.182+76C>T MANE Select	NP_006403.2:n.182+76C>T
NM_001012727.2:c.182+76C>T	NP_001012745.1:n.182+76C>T