Canonical Allele Identifier: CA201623249
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs535078102
gnomAD v2: 9-139568034-G-A
gnomAD v3: 9-136673582-G-A
gnomAD v4: 9-136673582-G-A
MyVariant Identifiers: chr9:g.139568034G>A (hg19) chr9:g.136673582G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673582G>A , CM000671.2:g.136673582G>A GRCh38
NC_000009.11:g.139568034G>A , CM000671.1:g.139568034G>A GRCh37
NC_000009.10:g.138687855G>A NCBI36
NG_008090.1:g.18878C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.*170C>T MANE Select ENSP00000360761.2:n.*170C>T
ENST00000371694.7:c.*170C>T ENSP00000360759.3:n.*170C>T
ENST00000371696.6:c.*170C>T ENSP00000360761.2:n.*170C>T
ENST00000538402.1:c.*170C>T ENSP00000438919.1:n.*170C>T
NM_001012727.1:c.*170C>T NP_001012745.1:n.*170C>T
NM_006412.3:c.*170C>T NP_006403.2:n.*170C>T
NM_006412.4:c.*170C>T MANE Select NP_006403.2:n.*170C>T
NM_001012727.2:c.*170C>T NP_001012745.1:n.*170C>T
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