Canonical Allele Identifier: CA497600579
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.6904926G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001607G>A , CM000679.2:g.7001607G>A GRCh38
NC_000017.10:g.6904926G>A , CM000679.1:g.6904926G>A GRCh37
NC_000017.9:g.6845650G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.957G>A (ALOX12) MANE Select ENSP00000251535.6:p.Gln319=
ENST00000251535.10:c.957G>A (ALOX12) ENSP00000251535.6:p.Gln319=
NM_000697.2:c.957G>A (ALOX12) NP_000688.2:p.Gln319=
NR_040089.1:n.233+8189C>T (ALOX12-AS1)
XM_011523780.1:c.1107G>A (ALOX12) XP_011522082.1:p.Gln369=
XM_011523780.2:c.1107G>A (ALOX12) XP_011522082.1:p.Gln369=
NM_000697.3:c.957G>A (ALOX12) MANE Select NP_000688.2:p.Gln319=
Search 100 bp 5'
Search 100 bp 3'