Canonical Allele Identifier: CA823936403
Gene: AGPAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1359282744
gnomAD v3: 6-32177693-C-A
gnomAD v4: 6-32177693-C-A
MyVariant Identifiers: chr6:g.32145470C>A (hg19) chr6:g.32177693C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32177693C>A , CM000668.2:g.32177693C>A GRCh38
NC_000006.11:g.32145470C>A , CM000668.1:g.32145470C>A GRCh37
NC_000006.10:g.32253448C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000336984.6:c.-10+308G>T ENSP00000337463.6:n.-10+308G>T
ENST00000395497.5:c.-159G>T ENSP00000378875.1:n.-159G>T
NM_032741.4:c.-10+308G>T NP_116130.2:n.-10+308G>T
XM_011514234.1:c.-159G>T XP_011512536.1:n.-159G>T
XM_005248806.2:c.-469G>T XP_005248863.1:n.-469G>T
NM_032741.5:c.-10+308G>T NP_116130.2:n.-10+308G>T
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