Canonical Allele Identifier: CA136908860
Gene: AGPAT1 HGNC NCBI

Linked Data

dbSNP Id: rs545368482
gnomAD v3: 6-32177908-A-G
gnomAD v4: 6-32177908-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32177908A>G , CM000668.2:g.32177908A>G GRCh38
NC_000006.11:g.32145685A>G , CM000668.1:g.32145685A>G GRCh37
NC_000006.10:g.32253663A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000336984.6:c.-10+93T>C ENSP00000337463.6:n.-10+93T>C
NM_032741.4:c.-10+93T>C NP_116130.2:n.-10+93T>C
NM_032741.5:c.-10+93T>C NP_116130.2:n.-10+93T>C