Canonical Allele Identifier: CA397738410
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1321896069
gnomAD v2: 17-6900346-G-T
gnomAD v4: 17-6997027-G-T
MyVariant Identifiers: chr17:g.6900346G>T (hg19) chr17:g.6997027G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6997027G>T , CM000679.2:g.6997027G>T GRCh38
NC_000017.10:g.6900346G>T , CM000679.1:g.6900346G>T GRCh37
NC_000017.9:g.6841070G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.337G>T (ALOX12) MANE Select ENSP00000251535.6:p.Ala113Ser
ENST00000251535.10:c.337G>T (ALOX12) ENSP00000251535.6:p.Ala113Ser
ENST00000480801.1:c.46G>T (ALOX12) ENSP00000467033.1:p.Ala16Ser
NM_000697.2:c.337G>T (ALOX12) NP_000688.2:p.Ala113Ser
NR_040089.1:n.234-11487C>A (ALOX12-AS1)
XM_011523780.1:c.694G>T (ALOX12) XP_011522082.1:p.Ala232Ser
XM_011523780.2:c.694G>T (ALOX12) XP_011522082.1:p.Ala232Ser
NM_000697.3:c.337G>T (ALOX12) MANE Select NP_000688.2:p.Ala113Ser
Search 100 bp 5'
Search 100 bp 3'