Canonical Allele Identifier: CA566372832
Gene: AGPAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1391618584
gnomAD v2: 6-32145543-C-T
gnomAD v3: 6-32177766-C-T
gnomAD v4: 6-32177766-C-T
MyVariant Identifiers: chr6:g.32145543C>T (hg19) chr6:g.32177766C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32177766C>T , CM000668.2:g.32177766C>T GRCh38
NC_000006.11:g.32145543C>T , CM000668.1:g.32145543C>T GRCh37
NC_000006.10:g.32253521C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000336984.6:c.-10+235G>A ENSP00000337463.6:n.-10+235G>A
ENST00000395497.5:c.-232G>A ENSP00000378875.1:n.-232G>A
NM_032741.4:c.-10+235G>A NP_116130.2:n.-10+235G>A
XM_011514234.1:c.-232G>A XP_011512536.1:n.-232G>A
NM_032741.5:c.-10+235G>A NP_116130.2:n.-10+235G>A
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