Canonical Allele Identifier: CA136908771
Gene: AGPAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1034263008
gnomAD v2: 6-32145518-T-C
gnomAD v3: 6-32177741-T-C
gnomAD v4: 6-32177741-T-C
MyVariant Identifiers: chr6:g.32145518T>C (hg19) chr6:g.32177741T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32177741T>C , CM000668.2:g.32177741T>C GRCh38
NC_000006.11:g.32145518T>C , CM000668.1:g.32145518T>C GRCh37
NC_000006.10:g.32253496T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000336984.6:c.-10+260A>G ENSP00000337463.6:n.-10+260A>G
ENST00000395497.5:c.-207A>G ENSP00000378875.1:n.-207A>G
NM_032741.4:c.-10+260A>G NP_116130.2:n.-10+260A>G
XM_011514234.1:c.-207A>G XP_011512536.1:n.-207A>G
XM_005248806.2:c.-517A>G XP_005248863.1:n.-517A>G
NM_032741.5:c.-10+260A>G NP_116130.2:n.-10+260A>G
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