Canonical Allele Identifier: CA397990572
Gene: ALOX12B HGNC NCBI

Linked Data

gnomAD v4: 17-8076263-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8076263G>C , CM000679.2:g.8076263G>C GRCh38
NC_000017.10:g.7979581G>C , CM000679.1:g.7979581G>C GRCh37
NC_000017.9:g.7920306G>C NCBI36
NG_007099.1:g.16441C>G
NG_007099.2:g.16454C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1444C>G MANE Select ENSP00000497784.1:p.Pro482Ala
ENST00000649809.1:c.508C>G ENSP00000496845.1:p.Pro170Ala
ENST00000319144.4:c.1444C>G ENSP00000315167.4:p.Pro482Ala
ENST00000577351.5:n.391C>G
ENST00000583276.5:n.828C>G
NM_001139.2:c.1444C>G NP_001130.1:p.Pro482Ala
NM_001139.3:c.1444C>G MANE Select NP_001130.1:p.Pro482Ala