Canonical Allele Identifier: CA823936424
Gene: AGPAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1352126160
gnomAD v3: 6-32177913-G-C
gnomAD v4: 6-32177913-G-C
MyVariant Identifiers: chr6:g.32145690G>C (hg19) chr6:g.32177913G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32177913G>C , CM000668.2:g.32177913G>C GRCh38
NC_000006.11:g.32145690G>C , CM000668.1:g.32145690G>C GRCh37
NC_000006.10:g.32253668G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000336984.6:c.-10+88C>G ENSP00000337463.6:n.-10+88C>G
NM_032741.4:c.-10+88C>G NP_116130.2:n.-10+88C>G
NM_032741.5:c.-10+88C>G NP_116130.2:n.-10+88C>G
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