Canonical Allele Identifier: CA136908716
Gene: AGPAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1039598644
MyVariant Identifiers: chr6:g.32145429C>G (hg19) chr6:g.32177652C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32177652C>G , CM000668.2:g.32177652C>G GRCh38
NC_000006.11:g.32145429C>G , CM000668.1:g.32145429C>G GRCh37
NC_000006.10:g.32253407C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000336984.6:c.-10+349G>C ENSP00000337463.6:n.-10+349G>C
ENST00000395497.5:c.-118G>C ENSP00000378875.1:n.-118G>C
NM_032741.4:c.-10+349G>C NP_116130.2:n.-10+349G>C
XM_011514234.1:c.-118G>C XP_011512536.1:n.-118G>C
XM_005248806.2:c.-428G>C XP_005248863.1:n.-428G>C
NM_032741.5:c.-10+349G>C NP_116130.2:n.-10+349G>C
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