Canonical Allele Identifier: CA497600683
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1908722268
gnomAD v4: 17-7001748-G-C
MyVariant Identifiers: chr17:g.6905067G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001748G>C , CM000679.2:g.7001748G>C GRCh38
NC_000017.10:g.6905067G>C , CM000679.1:g.6905067G>C GRCh37
NC_000017.9:g.6845791G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.1098G>C (ALOX12) MANE Select ENSP00000251535.6:p.Leu366=
ENST00000251535.10:c.1098G>C (ALOX12) ENSP00000251535.6:p.Leu366=
NM_000697.2:c.1098G>C (ALOX12) NP_000688.2:p.Leu366=
NR_040089.1:n.233+8048C>G (ALOX12-AS1)
XM_011523780.1:c.1248G>C (ALOX12) XP_011522082.1:p.Leu416=
XM_011523780.2:c.1248G>C (ALOX12) XP_011522082.1:p.Leu416=
NM_000697.3:c.1098G>C (ALOX12) MANE Select NP_000688.2:p.Leu366=