Canonical Allele Identifier: CA823936435
Gene: AGPAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1481076918
gnomAD v3: 6-32177970-T-TC
gnomAD v4: 6-32177970-T-TC
MyVariant Identifiers: chr6:g.32145747_32145748insC (hg19) chr6:g.32177970_32177971insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32177973dup , CM000668.2:g.32177973dup GRCh38
NC_000006.11:g.32145750dup , CM000668.1:g.32145750dup GRCh37
NC_000006.10:g.32253728dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000336984.6:c.-10+30dup ENSP00000337463.6:n.-10+30dup
NM_032741.4:c.-10+30dup NP_116130.2:n.-10+30dup
NM_032741.5:c.-10+30dup NP_116130.2:n.-10+30dup
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