Canonical Allele Identifier: CA136908867
Gene: AGPAT1 HGNC NCBI

Linked Data

dbSNP Id: rs36022314
gnomAD v2: 6-32145688-TA-T
gnomAD v3: 6-32177911-TA-T
gnomAD v4: 6-32177911-TA-T
MyVariant Identifiers: chr6:g.32145689del (hg19) chr6:g.32177912del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32177912del , CM000668.2:g.32177912del GRCh38
NC_000006.11:g.32145689del , CM000668.1:g.32145689del GRCh37
NC_000006.10:g.32253667del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000336984.6:c.-10+89del ENSP00000337463.6:n.-10+89del
NM_032741.4:c.-10+89del NP_116130.2:n.-10+89del
NM_032741.5:c.-10+89del NP_116130.2:n.-10+89del
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