Canonical Allele Identifier: CA398000053
Gene: ALOX12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7989513G>A (hg19) chr17:g.8086195G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086195G>A , CM000679.2:g.8086195G>A GRCh38
NC_000017.10:g.7989513G>A , CM000679.1:g.7989513G>A GRCh37
NC_000017.9:g.7930238G>A NCBI36
NG_007099.1:g.6509C>T
NG_007099.2:g.6522C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.173C>T MANE Select ENSP00000497784.1:p.Pro58Leu
ENST00000319144.4:c.173C>T ENSP00000315167.4:p.Pro58Leu
NM_001139.2:c.173C>T NP_001130.1:p.Pro58Leu
NM_001139.3:c.173C>T MANE Select NP_001130.1:p.Pro58Leu
Search 100 bp 5'
Search 100 bp 3'