Canonical Allele Identifier: CA772442007
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs1275376818
MyVariant Identifiers: chr17:g.4539505C>T (hg19) chr17:g.4636210C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4636210C>T , CM000679.2:g.4636210C>T GRCh38
NC_000017.10:g.4539505C>T , CM000679.1:g.4539505C>T GRCh37
NC_000017.9:g.4486254C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.952-242G>A MANE Select ENSP00000293761.3:n.952-242G>A
ENST00000570836.6:c.952-242G>A ENSP00000458832.1:n.952-242G>A
ENST00000293761.7:c.952-242G>A ENSP00000293761.3:n.952-242G>A
ENST00000570836.5:c.952-242G>A ENSP00000458832.1:n.952-242G>A
ENST00000574640.1:c.835-242G>A ENSP00000460483.1:n.835-242G>A
NM_001140.3:c.952-242G>A NP_001131.3:n.952-242G>A
NM_001140.4:c.952-242G>A NP_001131.3:n.952-242G>A
NM_001140.5:c.952-242G>A MANE Select NP_001131.3:n.952-242G>A
Search 100 bp 5'
Search 100 bp 3'