Canonical Allele Identifier: CA397999737
Gene: ALOX12B HGNC NCBI

Linked Data

dbSNP Id: rs1466188561
COSMIC: COSM3523722 COSM3523723
MyVariant Identifiers: chr17:g.7989454G>A (hg19) chr17:g.8086136G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086136G>A , CM000679.2:g.8086136G>A GRCh38
NC_000017.10:g.7989454G>A , CM000679.1:g.7989454G>A GRCh37
NC_000017.9:g.7930179G>A NCBI36
NG_007099.1:g.6568C>T
NG_007099.2:g.6581C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.232C>T MANE Select ENSP00000497784.1:p.Pro78Ser
ENST00000319144.4:c.232C>T ENSP00000315167.4:p.Pro78Ser
NM_001139.2:c.232C>T NP_001130.1:p.Pro78Ser
NM_001139.3:c.232C>T MANE Select NP_001130.1:p.Pro78Ser
Search 100 bp 5'
Search 100 bp 3'