Canonical Allele Identifier: CA397999709
Gene: ALOX12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7989449C>A (hg19) chr17:g.8086131C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086131C>A , CM000679.2:g.8086131C>A GRCh38
NC_000017.10:g.7989449C>A , CM000679.1:g.7989449C>A GRCh37
NC_000017.9:g.7930174C>A NCBI36
NG_007099.1:g.6573G>T
NG_007099.2:g.6586G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.237G>T MANE Select ENSP00000497784.1:p.Lys79Asn
ENST00000319144.4:c.237G>T ENSP00000315167.4:p.Lys79Asn
NM_001139.2:c.237G>T NP_001130.1:p.Lys79Asn
NM_001139.3:c.237G>T MANE Select NP_001130.1:p.Lys79Asn
Search 100 bp 5'
Search 100 bp 3'