Canonical Allele Identifier: CA397998942

Gene: ALOX12B

Linked Data

• dbSNP Id: rs1598184293
• MyVariant Identifiers: chr17:g.7989358T>G (hg19) ; chr17:g.8086040T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8086040T>G , CM000679.2:g.8086040T>G	GRCh38
NC_000017.10:g.7989358T>G , CM000679.1:g.7989358T>G	GRCh37
NC_000017.9:g.7930083T>G	NCBI36
NG_007099.1:g.6664A>C
NG_007099.2:g.6677A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.328A>C MANE Select	ENSP00000497784.1:p.Thr110Pro
ENST00000319144.4:c.328A>C	ENSP00000315167.4:p.Thr110Pro
NM_001139.2:c.328A>C	NP_001130.1:p.Thr110Pro
NM_001139.3:c.328A>C MANE Select	NP_001130.1:p.Thr110Pro