Canonical Allele Identifier: CA40858021
Gene: LYPD9P HGNC NCBI
OR14I1 HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.248697340A>C
GRCh37 chr1:g.248860641A>C
gnomAD v2:
1:248860641 A / C
gnomAD v3:
1:248697340 A / C
gnomAD v4:
chr1-248697340-A-C
Joint Max Group AF 0.29094693 (AFR)
Genomes Max Group AF 0.29094693 (AFR)
Exomes Max Group AF 0.03553614 (NFE)
dbSNP:
4916176
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.248697340A>C , CM000663.2:g.248697340A>C GRCh38
NC_000001.10:g.248860641A>C , CM000663.1:g.248860641A>C GRCh37
NC_000001.9:g.246927264A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437830.4:n.480+133A>C (LYPD9P)
ENST00000611154.3:n.469+133A>C (LYPD9P)
ENST00000636515.1:n.244+133A>C (LYPD9P)
ENST00000651827.1:c.258+1507T>G ENSP00000498451.1:n.258+1507T>G
NR_125950.1:n.146+133A>C (LYPD9P)
XM_005273131.3:c.31+1507T>G (OR14I1) XP_005273188.1:n.31+1507T>G
XR_949140.1:n.53+1507T>G (OR14I1)
XR_949143.1:n.53+1507T>G (OR14I1)
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