Canonical Allele Identifier: CA8306627
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs763623532
ExAC: 17:4534941 T / C
gnomAD v2: 17-4534941-T-C
gnomAD v3: 17-4631646-T-C
gnomAD v4: 17-4631646-T-C
MyVariant Identifiers: chr17:g.4534941T>C (hg19) chr17:g.4631646T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631646T>C , CM000679.2:g.4631646T>C GRCh38
NC_000017.10:g.4534941T>C , CM000679.1:g.4534941T>C GRCh37
NC_000017.9:g.4481690T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1943A>G MANE Select ENSP00000293761.3:p.Tyr648Cys
ENST00000570836.6:c.1943A>G ENSP00000458832.1:p.Tyr648Cys
ENST00000293761.7:c.1943A>G ENSP00000293761.3:p.Tyr648Cys
ENST00000570836.5:c.1943A>G ENSP00000458832.1:p.Tyr648Cys
ENST00000574640.1:c.1826A>G ENSP00000460483.1:p.Tyr609Cys
NM_001140.3:c.1943A>G NP_001131.3:p.Tyr648Cys
NM_001140.4:c.1943A>G NP_001131.3:p.Tyr648Cys
NM_001140.5:c.1943A>G MANE Select NP_001131.3:p.Tyr648Cys
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