Canonical Allele Identifier: CA772437136
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs1459710168
MyVariant Identifiers: chr17:g.4534468G>A (hg19) chr17:g.4631173G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631173G>A , CM000679.2:g.4631173G>A GRCh38
NC_000017.10:g.4534468G>A , CM000679.1:g.4534468G>A GRCh37
NC_000017.9:g.4481217G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*427C>T MANE Select ENSP00000293761.3:n.*427C>T
ENST00000293761.7:c.*427C>T ENSP00000293761.3:n.*427C>T
ENST00000570836.5:c.*427C>T ENSP00000458832.1:n.*427C>T
NM_001140.3:c.*427C>T NP_001131.3:n.*427C>T
NM_001140.4:c.*427C>T NP_001131.3:n.*427C>T
NM_001140.5:c.*427C>T MANE Select NP_001131.3:n.*427C>T
Search 100 bp 5'
Search 100 bp 3'