Canonical Allele Identifier: CA8306689
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs762523931
ExAC: 17:4535248 T / C
gnomAD v2: 17-4535248-T-C
gnomAD v3: 17-4631953-T-C
gnomAD v4: 17-4631953-T-C
MyVariant Identifiers: chr17:g.4535248T>C (hg19) chr17:g.4631953T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631953T>C , CM000679.2:g.4631953T>C GRCh38
NC_000017.10:g.4535248T>C , CM000679.1:g.4535248T>C GRCh37
NC_000017.9:g.4481997T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1745A>G MANE Select ENSP00000293761.3:p.Asn582Ser
ENST00000570836.6:c.1745A>G ENSP00000458832.1:p.Asn582Ser
ENST00000293761.7:c.1745A>G ENSP00000293761.3:p.Asn582Ser
ENST00000570836.5:c.1745A>G ENSP00000458832.1:p.Asn582Ser
ENST00000574640.1:c.1628A>G ENSP00000460483.1:p.Asn543Ser
NM_001140.3:c.1745A>G NP_001131.3:p.Asn582Ser
NM_001140.4:c.1745A>G NP_001131.3:p.Asn582Ser
NM_001140.5:c.1745A>G MANE Select NP_001131.3:p.Asn582Ser
Search 100 bp 5'
Search 100 bp 3'