Canonical Allele Identifier: CA2692654654
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136676798-C-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136676798C>G , CM000671.2:g.136676798C>G GRCh38
NC_000009.11:g.139571250C>G , CM000671.1:g.139571250C>G GRCh37
NC_000009.10:g.138691071C>G NCBI36
NG_008090.1:g.15662G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.493-118G>C MANE Select ENSP00000360761.2:n.493-118G>C
ENST00000371694.7:c.492+163G>C ENSP00000360759.3:n.492+163G>C
ENST00000371696.6:c.493-118G>C ENSP00000360761.2:n.493-118G>C
ENST00000472820.1:n.421-118G>C
ENST00000538402.1:c.493-118G>C ENSP00000438919.1:n.493-118G>C
NM_001012727.1:c.492+163G>C NP_001012745.1:n.492+163G>C
NM_006412.3:c.493-118G>C NP_006403.2:n.493-118G>C
NM_006412.4:c.493-118G>C MANE Select NP_006403.2:n.493-118G>C
NM_001012727.2:c.492+163G>C NP_001012745.1:n.492+163G>C
Search 100 bp 5'
Search 100 bp 3'