Canonical Allele Identifier: CA8306619
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs776815094
ExAC: 17:4534910 G / C
gnomAD v2: 17-4534910-G-C
gnomAD v4: 17-4631615-G-C
MyVariant Identifiers: chr17:g.4534910G>C (hg19) chr17:g.4631615G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631615G>C , CM000679.2:g.4631615G>C GRCh38
NC_000017.10:g.4534910G>C , CM000679.1:g.4534910G>C GRCh37
NC_000017.9:g.4481659G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1974C>G MANE Select ENSP00000293761.3:p.Asn658Lys
ENST00000570836.6:c.1974C>G ENSP00000458832.1:p.Asn658Lys
ENST00000293761.7:c.1974C>G ENSP00000293761.3:p.Asn658Lys
ENST00000570836.5:c.1974C>G ENSP00000458832.1:p.Asn658Lys
ENST00000574640.1:c.1857C>G ENSP00000460483.1:p.Asn619Lys
NM_001140.3:c.1974C>G NP_001131.3:p.Asn658Lys
NM_001140.4:c.1974C>G NP_001131.3:p.Asn658Lys
NM_001140.5:c.1974C>G MANE Select NP_001131.3:p.Asn658Lys
Search 100 bp 5'
Search 100 bp 3'