Canonical Allele Identifier: CA823936397
Gene: AGPAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1462466184
MyVariant Identifiers: chr6:g.32145413A>T (hg19) chr6:g.32177636A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32177636A>T , CM000668.2:g.32177636A>T GRCh38
NC_000006.11:g.32145413A>T , CM000668.1:g.32145413A>T GRCh37
NC_000006.10:g.32253391A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000336984.6:c.-10+365T>A ENSP00000337463.6:n.-10+365T>A
ENST00000395497.5:c.-102T>A ENSP00000378875.1:n.-102T>A
NM_032741.4:c.-10+365T>A NP_116130.2:n.-10+365T>A
XM_011514234.1:c.-102T>A XP_011512536.1:n.-102T>A
XM_005248806.2:c.-412T>A XP_005248863.1:n.-412T>A
NM_032741.5:c.-10+365T>A NP_116130.2:n.-10+365T>A
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