Canonical Allele Identifier: CA2635962196
Gene: ALOX12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086296dup , CM000679.2:g.8086296dup GRCh38
NC_000017.10:g.7989614dup , CM000679.1:g.7989614dup GRCh37
NC_000017.9:g.7930339dup NCBI36
NG_007099.1:g.6408dup
NG_007099.2:g.6421dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.148-76dup MANE Select ENSP00000497784.1:n.148-76dup
ENST00000319144.4:c.148-76dup ENSP00000315167.4:n.148-76dup
NM_001139.2:c.148-76dup NP_001130.1:n.148-76dup
NM_001139.3:c.148-76dup MANE Select NP_001130.1:n.148-76dup