Canonical Allele Identifier: CA2635746089
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

gnomAD v4: 17-6996778-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996778T>C , CM000679.2:g.6996778T>C GRCh38
NC_000017.10:g.6900097T>C , CM000679.1:g.6900097T>C GRCh37
NC_000017.9:g.6840821T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000251535.11:c.136-48T>C (ALOX12) MANE Select ENSP00000251535.6:n.136-48T>C
ENST00000251535.10:c.136-48T>C (ALOX12) ENSP00000251535.6:n.136-48T>C
NM_000697.2:c.136-48T>C (ALOX12) NP_000688.2:n.136-48T>C
NR_040089.1:n.234-11238A>G (ALOX12-AS1)
XM_011523780.1:c.493-48T>C (ALOX12) XP_011522082.1:n.493-48T>C
XM_011523780.2:c.493-48T>C (ALOX12) XP_011522082.1:n.493-48T>C
NM_000697.3:c.136-48T>C (ALOX12) MANE Select NP_000688.2:n.136-48T>C
Search 100 bp 5'
Search 100 bp 3'