Canonical Allele Identifier: CA1087506003
Gene: AGPAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1785725408
gnomAD v3: 6-32177925-T-C
gnomAD v4: 6-32177925-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32177925T>C , CM000668.2:g.32177925T>C GRCh38
NC_000006.11:g.32145702T>C , CM000668.1:g.32145702T>C GRCh37
NC_000006.10:g.32253680T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000336984.6:c.-10+76A>G ENSP00000337463.6:n.-10+76A>G
NM_032741.4:c.-10+76A>G NP_116130.2:n.-10+76A>G
NM_032741.5:c.-10+76A>G NP_116130.2:n.-10+76A>G