Canonical Allele Identifier: CA774566909

Gene: ALOX12 ALOX12-AS1

Linked Data

• dbSNP Id: rs1371496289
• MyVariant Identifiers: chr17:g.6905224T>C (hg19) ; chr17:g.7001905T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7001905T>C , CM000679.2:g.7001905T>C	GRCh38
NC_000017.10:g.6905224T>C , CM000679.1:g.6905224T>C	GRCh37
NC_000017.9:g.6845948T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.1161+94T>C (ALOX12) MANE Select	ENSP00000251535.6:n.1161+94T>C
ENST00000251535.10:c.1161+94T>C (ALOX12)	ENSP00000251535.6:n.1161+94T>C
NM_000697.2:c.1161+94T>C (ALOX12)	NP_000688.2:n.1161+94T>C
NR_040089.1:n.233+7891A>G (ALOX12-AS1)
XM_011523780.1:c.1311+94T>C (ALOX12)	XP_011522082.1:n.1311+94T>C
XM_011523780.2:c.1311+94T>C (ALOX12)	XP_011522082.1:n.1311+94T>C
NM_000697.3:c.1161+94T>C (ALOX12) MANE Select	NP_000688.2:n.1161+94T>C