Canonical Allele Identifier: CA136908721
Gene: AGPAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1001880223
gnomAD v2: 6-32145435-T-G
gnomAD v3: 6-32177658-T-G
gnomAD v4: 6-32177658-T-G
MyVariant Identifiers: chr6:g.32145435T>G (hg19) chr6:g.32177658T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32177658T>G , CM000668.2:g.32177658T>G GRCh38
NC_000006.11:g.32145435T>G , CM000668.1:g.32145435T>G GRCh37
NC_000006.10:g.32253413T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000336984.6:c.-10+343A>C ENSP00000337463.6:n.-10+343A>C
ENST00000395497.5:c.-124A>C ENSP00000378875.1:n.-124A>C
NM_032741.4:c.-10+343A>C NP_116130.2:n.-10+343A>C
XM_011514234.1:c.-124A>C XP_011512536.1:n.-124A>C
XM_005248806.2:c.-434A>C XP_005248863.1:n.-434A>C
NM_032741.5:c.-10+343A>C NP_116130.2:n.-10+343A>C
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