Canonical Allele Identifier: CA2635961555
Gene: ALOX12B HGNC NCBI

Linked Data

gnomAD v4: 17-8085996-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8085996G>A , CM000679.2:g.8085996G>A GRCh38
NC_000017.10:g.7989314G>A , CM000679.1:g.7989314G>A GRCh37
NC_000017.9:g.7930039G>A NCBI36
NG_007099.1:g.6708C>T
NG_007099.2:g.6721C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.352+20C>T MANE Select ENSP00000497784.1:n.352+20C>T
ENST00000319144.4:c.352+20C>T ENSP00000315167.4:n.352+20C>T
NM_001139.2:c.352+20C>T NP_001130.1:n.352+20C>T
NM_001139.3:c.352+20C>T MANE Select NP_001130.1:n.352+20C>T
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