Canonical Allele Identifier: CA8367331
Gene: ALOX12B HGNC NCBI

Linked Data

dbSNP Id: rs757391567
ExAC: 17:7979949 G / C
gnomAD v2: 17-7979949-G-C
gnomAD v3: 17-8076631-G-C
gnomAD v4: 17-8076631-G-C
MyVariant Identifiers: chr17:g.7979949G>C (hg19) chr17:g.8076631G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8076631G>C , CM000679.2:g.8076631G>C GRCh38
NC_000017.10:g.7979949G>C , CM000679.1:g.7979949G>C GRCh37
NC_000017.9:g.7920674G>C NCBI36
NG_007099.1:g.16073C>G
NG_007099.2:g.16086C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1362+26C>G MANE Select ENSP00000497784.1:n.1362+26C>G
ENST00000649809.1:c.426+26C>G ENSP00000496845.1:n.426+26C>G
ENST00000319144.4:c.1362+26C>G ENSP00000315167.4:n.1362+26C>G
ENST00000577351.5:n.309+26C>G
ENST00000583276.5:n.746+26C>G
ENST00000584116.1:n.618+26C>G
NM_001139.2:c.1362+26C>G NP_001130.1:n.1362+26C>G
NM_001139.3:c.1362+26C>G MANE Select NP_001130.1:n.1362+26C>G
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