Canonical Allele Identifier: CA8333411

Gene: ALOX12 ALOX12-AS1

Linked Data

• dbSNP Id: rs778331954
• ExAC: 17:6905136 T / C
• gnomAD v2: 17-6905136-T-C
• gnomAD v3: 17-7001817-T-C
• gnomAD v4: 17-7001817-T-C
• MyVariant Identifiers: chr17:g.6905136T>C (hg19) ; chr17:g.7001817T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7001817T>C , CM000679.2:g.7001817T>C	GRCh38
NC_000017.10:g.6905136T>C , CM000679.1:g.6905136T>C	GRCh37
NC_000017.9:g.6845860T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.1161+6T>C (ALOX12) MANE Select	ENSP00000251535.6:n.1161+6T>C
ENST00000251535.10:c.1161+6T>C (ALOX12)	ENSP00000251535.6:n.1161+6T>C
NM_000697.2:c.1161+6T>C (ALOX12)	NP_000688.2:n.1161+6T>C
NR_040089.1:n.233+7979A>G (ALOX12-AS1)
XM_011523780.1:c.1311+6T>C (ALOX12)	XP_011522082.1:n.1311+6T>C
XM_011523780.2:c.1311+6T>C (ALOX12)	XP_011522082.1:n.1311+6T>C
NM_000697.3:c.1161+6T>C (ALOX12) MANE Select	NP_000688.2:n.1161+6T>C