Canonical Allele Identifier: CA397999424
Gene: ALOX12B HGNC NCBI

Linked Data

dbSNP Id: rs757596043
MyVariant Identifiers: chr17:g.7989420A>C (hg19) chr17:g.8086102A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086102A>C , CM000679.2:g.8086102A>C GRCh38
NC_000017.10:g.7989420A>C , CM000679.1:g.7989420A>C GRCh37
NC_000017.9:g.7930145A>C NCBI36
NG_007099.1:g.6602T>G
NG_007099.2:g.6615T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.266T>G MANE Select ENSP00000497784.1:p.Ile89Ser
ENST00000319144.4:c.266T>G ENSP00000315167.4:p.Ile89Ser
NM_001139.2:c.266T>G NP_001130.1:p.Ile89Ser
NM_001139.3:c.266T>G MANE Select NP_001130.1:p.Ile89Ser
Search 100 bp 5'
Search 100 bp 3'