Canonical Allele Identifier: CA2635957568
Gene: ALOX12B HGNC NCBI

Linked Data

gnomAD v4: 17-8075522-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8075522C>A , CM000679.2:g.8075522C>A GRCh38
NC_000017.10:g.7978840C>A , CM000679.1:g.7978840C>A GRCh37
NC_000017.9:g.7919565C>A NCBI36
NG_007099.1:g.17182G>T
NG_007099.2:g.17195G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647874.1:c.1654+73G>T MANE Select ENSP00000497784.1:n.1654+73G>T
ENST00000649809.1:c.718+73G>T ENSP00000496845.1:n.718+73G>T
ENST00000319144.4:c.1654+73G>T ENSP00000315167.4:n.1654+73G>T
ENST00000577351.5:n.479+653G>T
NM_001139.2:c.1654+73G>T NP_001130.1:n.1654+73G>T
NM_001139.3:c.1654+73G>T MANE Select NP_001130.1:n.1654+73G>T
Search 100 bp 5'
Search 100 bp 3'