Canonical Allele Identifier: CA497600728
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.6905100G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001781G>T , CM000679.2:g.7001781G>T GRCh38
NC_000017.10:g.6905100G>T , CM000679.1:g.6905100G>T GRCh37
NC_000017.9:g.6845824G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.1131G>T (ALOX12) MANE Select ENSP00000251535.6:p.Arg377=
ENST00000251535.10:c.1131G>T (ALOX12) ENSP00000251535.6:p.Arg377=
NM_000697.2:c.1131G>T (ALOX12) NP_000688.2:p.Arg377=
NR_040089.1:n.233+8015C>A (ALOX12-AS1)
XM_011523780.1:c.1281G>T (ALOX12) XP_011522082.1:p.Arg427=
XM_011523780.2:c.1281G>T (ALOX12) XP_011522082.1:p.Arg427=
NM_000697.3:c.1131G>T (ALOX12) MANE Select NP_000688.2:p.Arg377=