Canonical Allele Identifier: CA2246104396
Gene: ALOX12B HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086019T= , CM000679.2:g.8086019T= GRCh38
NC_000017.10:g.7989337T= , CM000679.1:g.7989337T= GRCh37
NC_000017.9:g.7930062T= NCBI36
NG_007099.1:g.6685A=
NG_007099.2:g.6698A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.349A= MANE Select ENSP00000497784.1:p.Thr117=
ENST00000319144.4:c.349A= ENSP00000315167.4:p.Thr117=
NM_001139.2:c.349A= NP_001130.1:p.Thr117=
NM_001139.3:c.349A= MANE Select NP_001130.1:p.Thr117=
Search 100 bp 5'
Search 100 bp 3'