Canonical Allele Identifier: CA2635962218
Gene: ALOX12B HGNC NCBI

Linked Data

gnomAD v4: 17-8086305-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086305C>A , CM000679.2:g.8086305C>A GRCh38
NC_000017.10:g.7989623C>A , CM000679.1:g.7989623C>A GRCh37
NC_000017.9:g.7930348C>A NCBI36
NG_007099.1:g.6399G>T
NG_007099.2:g.6412G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.148-85G>T MANE Select ENSP00000497784.1:n.148-85G>T
ENST00000319144.4:c.148-85G>T ENSP00000315167.4:n.148-85G>T
NM_001139.2:c.148-85G>T NP_001130.1:n.148-85G>T
NM_001139.3:c.148-85G>T MANE Select NP_001130.1:n.148-85G>T
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