Canonical Allele Identifier: CA497762919
Gene: ALOX12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7989413G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086095G>A , CM000679.2:g.8086095G>A GRCh38
NC_000017.10:g.7989413G>A , CM000679.1:g.7989413G>A GRCh37
NC_000017.9:g.7930138G>A NCBI36
NG_007099.1:g.6609C>T
NG_007099.2:g.6622C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.273C>T MANE Select ENSP00000497784.1:p.Ala91=
ENST00000319144.4:c.273C>T ENSP00000315167.4:p.Ala91=
NM_001139.2:c.273C>T NP_001130.1:p.Ala91=
NM_001139.3:c.273C>T MANE Select NP_001130.1:p.Ala91=
Search 100 bp 5'
Search 100 bp 3'