Canonical Allele Identifier: CA2635957553

Gene: ALOX12B

Linked Data

• gnomAD v4: 17-8075518-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8075518A>C , CM000679.2:g.8075518A>C	GRCh38
NC_000017.10:g.7978836A>C , CM000679.1:g.7978836A>C	GRCh37
NC_000017.9:g.7919561A>C	NCBI36
NG_007099.1:g.17186T>G
NG_007099.2:g.17199T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000647874.1:c.1654+77T>G MANE Select	ENSP00000497784.1:n.1654+77T>G
ENST00000649809.1:c.718+77T>G	ENSP00000496845.1:n.718+77T>G
ENST00000319144.4:c.1654+77T>G	ENSP00000315167.4:n.1654+77T>G
ENST00000577351.5:n.479+657T>G
NM_001139.2:c.1654+77T>G	NP_001130.1:n.1654+77T>G
NM_001139.3:c.1654+77T>G MANE Select	NP_001130.1:n.1654+77T>G