Canonical Allele Identifier: CA397999385
Gene: ALOX12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7989414G>T (hg19) chr17:g.8086096G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086096G>T , CM000679.2:g.8086096G>T GRCh38
NC_000017.10:g.7989414G>T , CM000679.1:g.7989414G>T GRCh37
NC_000017.9:g.7930139G>T NCBI36
NG_007099.1:g.6608C>A
NG_007099.2:g.6621C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.272C>A MANE Select ENSP00000497784.1:p.Ala91Asp
ENST00000319144.4:c.272C>A ENSP00000315167.4:p.Ala91Asp
NM_001139.2:c.272C>A NP_001130.1:p.Ala91Asp
NM_001139.3:c.272C>A MANE Select NP_001130.1:p.Ala91Asp
Search 100 bp 5'
Search 100 bp 3'