Canonical Allele Identifier: CA8367752
Gene: ALOX12B HGNC NCBI

Linked Data

dbSNP Id: rs749076126
ExAC: 17:7989566 G / T
gnomAD v2: 17-7989566-G-T
gnomAD v4: 17-8086248-G-T
MyVariant Identifiers: chr17:g.7989566G>T (hg19) chr17:g.8086248G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086248G>T , CM000679.2:g.8086248G>T GRCh38
NC_000017.10:g.7989566G>T , CM000679.1:g.7989566G>T GRCh37
NC_000017.9:g.7930291G>T NCBI36
NG_007099.1:g.6456C>A
NG_007099.2:g.6469C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.148-28C>A MANE Select ENSP00000497784.1:n.148-28C>A
ENST00000319144.4:c.148-28C>A ENSP00000315167.4:n.148-28C>A
NM_001139.2:c.148-28C>A NP_001130.1:n.148-28C>A
NM_001139.3:c.148-28C>A MANE Select NP_001130.1:n.148-28C>A
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