Canonical Allele Identifier: CA287375677

Gene: ALOX12 ALOX12-AS1

Linked Data

• dbSNP Id: rs968186808
• gnomAD v4: 17-7001873-T-A
• MyVariant Identifiers: chr17:g.6905192T>A (hg19) ; chr17:g.7001873T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7001873T>A , CM000679.2:g.7001873T>A	GRCh38
NC_000017.10:g.6905192T>A , CM000679.1:g.6905192T>A	GRCh37
NC_000017.9:g.6845916T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.1161+62T>A (ALOX12) MANE Select	ENSP00000251535.6:n.1161+62T>A
ENST00000251535.10:c.1161+62T>A (ALOX12)	ENSP00000251535.6:n.1161+62T>A
NM_000697.2:c.1161+62T>A (ALOX12)	NP_000688.2:n.1161+62T>A
NR_040089.1:n.233+7923A>T (ALOX12-AS1)
XM_011523780.1:c.1311+62T>A (ALOX12)	XP_011522082.1:n.1311+62T>A
XM_011523780.2:c.1311+62T>A (ALOX12)	XP_011522082.1:n.1311+62T>A
NM_000697.3:c.1161+62T>A (ALOX12) MANE Select	NP_000688.2:n.1161+62T>A