Canonical Allele Identifier: CA2692655493
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136687424-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687424C>A , CM000671.2:g.136687424C>A GRCh38
NC_000009.11:g.139581876C>A , CM000671.1:g.139581876C>A GRCh37
NC_000009.10:g.138701697C>A NCBI36
NG_008090.1:g.5036G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.-67G>T MANE Select ENSP00000360761.2:n.-67G>T
NM_001012727.1:c.-67G>T NP_001012745.1:n.-67G>T
NM_006412.3:c.-67G>T NP_006403.2:n.-67G>T
NM_006412.4:c.-67G>T MANE Select NP_006403.2:n.-67G>T
NM_001012727.2:c.-67G>T NP_001012745.1:n.-67G>T
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