Canonical Allele Identifier: CA566372837
Gene: AGPAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1356056653
gnomAD v2: 6-32145600-T-C
gnomAD v3: 6-32177823-T-C
gnomAD v4: 6-32177823-T-C
MyVariant Identifiers: chr6:g.32145600T>C (hg19) chr6:g.32177823T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32177823T>C , CM000668.2:g.32177823T>C GRCh38
NC_000006.11:g.32145600T>C , CM000668.1:g.32145600T>C GRCh37
NC_000006.10:g.32253578T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000336984.6:c.-10+178A>G ENSP00000337463.6:n.-10+178A>G
NM_032741.4:c.-10+178A>G NP_116130.2:n.-10+178A>G
XM_011514234.1:c.-289A>G XP_011512536.1:n.-289A>G
NM_032741.5:c.-10+178A>G NP_116130.2:n.-10+178A>G
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