Canonical Allele Identifier: CA397999637

Gene: ALOX12B

Linked Data

• dbSNP Id: rs1978297124
• MyVariant Identifiers: chr17:g.7989441C>G (hg19) ; chr17:g.8086123C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8086123C>G , CM000679.2:g.8086123C>G	GRCh38
NC_000017.10:g.7989441C>G , CM000679.1:g.7989441C>G	GRCh37
NC_000017.9:g.7930166C>G	NCBI36
NG_007099.1:g.6581G>C
NG_007099.2:g.6594G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.245G>C MANE Select	ENSP00000497784.1:p.Trp82Ser
ENST00000319144.4:c.245G>C	ENSP00000315167.4:p.Trp82Ser
NM_001139.2:c.245G>C	NP_001130.1:p.Trp82Ser
NM_001139.3:c.245G>C MANE Select	NP_001130.1:p.Trp82Ser