Canonical Allele Identifier: CA8367751
Gene: ALOX12B HGNC NCBI

Linked Data

dbSNP Id: rs773190505
ExAC: 17:7989564 G / C
gnomAD v2: 17-7989564-G-C
gnomAD v4: 17-8086246-G-C
MyVariant Identifiers: chr17:g.7989564G>C (hg19) chr17:g.8086246G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086246G>C , CM000679.2:g.8086246G>C GRCh38
NC_000017.10:g.7989564G>C , CM000679.1:g.7989564G>C GRCh37
NC_000017.9:g.7930289G>C NCBI36
NG_007099.1:g.6458C>G
NG_007099.2:g.6471C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.148-26C>G MANE Select ENSP00000497784.1:n.148-26C>G
ENST00000319144.4:c.148-26C>G ENSP00000315167.4:n.148-26C>G
NM_001139.2:c.148-26C>G NP_001130.1:n.148-26C>G
NM_001139.3:c.148-26C>G MANE Select NP_001130.1:n.148-26C>G
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