Canonical Allele Identifier: CA624675757
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1187601806
gnomAD v2: 17-6899890-C-T
gnomAD v3: 17-6996571-C-T
gnomAD v4: 17-6996571-C-T
MyVariant Identifiers: chr17:g.6899890C>T (hg19) chr17:g.6996571C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996571C>T , CM000679.2:g.6996571C>T GRCh38
NC_000017.10:g.6899890C>T , CM000679.1:g.6899890C>T GRCh37
NC_000017.9:g.6840614C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.136-255C>T (ALOX12) MANE Select ENSP00000251535.6:n.136-255C>T
ENST00000251535.10:c.136-255C>T (ALOX12) ENSP00000251535.6:n.136-255C>T
NM_000697.2:c.136-255C>T (ALOX12) NP_000688.2:n.136-255C>T
NR_040089.1:n.234-11031G>A (ALOX12-AS1)
XM_011523780.1:c.493-255C>T (ALOX12) XP_011522082.1:n.493-255C>T
XM_011523780.2:c.493-255C>T (ALOX12) XP_011522082.1:n.493-255C>T
NM_000697.3:c.136-255C>T (ALOX12) MANE Select NP_000688.2:n.136-255C>T
Search 100 bp 5'
Search 100 bp 3'