Canonical Allele Identifier: CA497599031
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

gnomAD v4: 17-6996903-G-A
MyVariant Identifiers: chr17:g.6900222G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996903G>A , CM000679.2:g.6996903G>A GRCh38
NC_000017.10:g.6900222G>A , CM000679.1:g.6900222G>A GRCh37
NC_000017.9:g.6840946G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.213G>A (ALOX12) MANE Select ENSP00000251535.6:p.Leu71=
ENST00000251535.10:c.213G>A (ALOX12) ENSP00000251535.6:p.Leu71=
NM_000697.2:c.213G>A (ALOX12) NP_000688.2:p.Leu71=
NR_040089.1:n.234-11363C>T (ALOX12-AS1)
XM_011523780.1:c.570G>A (ALOX12) XP_011522082.1:p.Leu190=
XM_011523780.2:c.570G>A (ALOX12) XP_011522082.1:p.Leu190=
NM_000697.3:c.213G>A (ALOX12) MANE Select NP_000688.2:p.Leu71=
Search 100 bp 5'
Search 100 bp 3'