Canonical Allele Identifier: CA287375730
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs141605190
gnomAD v3: 17-7001938-A-G
gnomAD v4: 17-7001938-A-G
MyVariant Identifiers: chr17:g.6905257A>G (hg19) chr17:g.7001938A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001938A>G , CM000679.2:g.7001938A>G GRCh38
NC_000017.10:g.6905257A>G , CM000679.1:g.6905257A>G GRCh37
NC_000017.9:g.6845981A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.1161+127A>G (ALOX12) MANE Select ENSP00000251535.6:n.1161+127A>G
ENST00000251535.10:c.1161+127A>G (ALOX12) ENSP00000251535.6:n.1161+127A>G
NM_000697.2:c.1161+127A>G (ALOX12) NP_000688.2:n.1161+127A>G
NR_040089.1:n.233+7858T>C (ALOX12-AS1)
XM_011523780.1:c.1311+127A>G (ALOX12) XP_011522082.1:n.1311+127A>G
XM_011523780.2:c.1311+127A>G (ALOX12) XP_011522082.1:n.1311+127A>G
NM_000697.3:c.1161+127A>G (ALOX12) MANE Select NP_000688.2:n.1161+127A>G
Search 100 bp 5'
Search 100 bp 3'