Canonical Allele Identifier: CA397748473
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1207958649
gnomAD v2: 17-6905042-A-C
gnomAD v4: 17-7001723-A-C
MyVariant Identifiers: chr17:g.6905042A>C (hg19) chr17:g.7001723A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001723A>C , CM000679.2:g.7001723A>C GRCh38
NC_000017.10:g.6905042A>C , CM000679.1:g.6905042A>C GRCh37
NC_000017.9:g.6845766A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.1073A>C (ALOX12) MANE Select ENSP00000251535.6:p.Gln358Pro
ENST00000251535.10:c.1073A>C (ALOX12) ENSP00000251535.6:p.Gln358Pro
NM_000697.2:c.1073A>C (ALOX12) NP_000688.2:p.Gln358Pro
NR_040089.1:n.233+8073T>G (ALOX12-AS1)
XM_011523780.1:c.1223A>C (ALOX12) XP_011522082.1:p.Gln408Pro
XM_011523780.2:c.1223A>C (ALOX12) XP_011522082.1:p.Gln408Pro
NM_000697.3:c.1073A>C (ALOX12) MANE Select NP_000688.2:p.Gln358Pro
Search 100 bp 5'
Search 100 bp 3'