Canonical Allele Identifier: CA2635959653
Gene: ALOX12B HGNC NCBI

Linked Data

gnomAD v4: 17-8076589-C-CT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8076590dup , CM000679.2:g.8076590dup GRCh38
NC_000017.10:g.7979908dup , CM000679.1:g.7979908dup GRCh37
NC_000017.9:g.7920633dup NCBI36
NG_007099.1:g.16114dup
NG_007099.2:g.16127dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1362+67dup MANE Select ENSP00000497784.1:n.1362+67dup
ENST00000649809.1:c.426+67dup ENSP00000496845.1:n.426+67dup
ENST00000319144.4:c.1362+67dup ENSP00000315167.4:n.1362+67dup
ENST00000577351.5:n.309+67dup
ENST00000583276.5:n.746+67dup
ENST00000584116.1:n.618+67dup
NM_001139.2:c.1362+67dup NP_001130.1:n.1362+67dup
NM_001139.3:c.1362+67dup MANE Select NP_001130.1:n.1362+67dup
Search 100 bp 5'
Search 100 bp 3'