Canonical Allele Identifier: CA397748772
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

gnomAD v4: 17-7001753-C-A
MyVariant Identifiers: chr17:g.6905072C>A (hg19) chr17:g.7001753C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001753C>A , CM000679.2:g.7001753C>A GRCh38
NC_000017.10:g.6905072C>A , CM000679.1:g.6905072C>A GRCh37
NC_000017.9:g.6845796C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.1103C>A (ALOX12) MANE Select ENSP00000251535.6:p.Ala368Asp
ENST00000251535.10:c.1103C>A (ALOX12) ENSP00000251535.6:p.Ala368Asp
NM_000697.2:c.1103C>A (ALOX12) NP_000688.2:p.Ala368Asp
NR_040089.1:n.233+8043G>T (ALOX12-AS1)
XM_011523780.1:c.1253C>A (ALOX12) XP_011522082.1:p.Ala418Asp
XM_011523780.2:c.1253C>A (ALOX12) XP_011522082.1:p.Ala418Asp
NM_000697.3:c.1103C>A (ALOX12) MANE Select NP_000688.2:p.Ala368Asp
Search 100 bp 5'
Search 100 bp 3'