Canonical Allele Identifier: CA201641657
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs553123602

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687413T>C , CM000671.2:g.136687413T>C GRCh38
NC_000009.11:g.139581865T>C , CM000671.1:g.139581865T>C GRCh37
NC_000009.10:g.138701686T>C NCBI36
NG_008090.1:g.5047A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.-56A>G MANE Select ENSP00000360761.2:n.-56A>G
ENST00000371696.6:c.-56A>G ENSP00000360761.2:n.-56A>G
NM_001012727.1:c.-56A>G NP_001012745.1:n.-56A>G
NM_006412.3:c.-56A>G NP_006403.2:n.-56A>G
NM_006412.4:c.-56A>G MANE Select NP_006403.2:n.-56A>G
NM_001012727.2:c.-56A>G NP_001012745.1:n.-56A>G