Canonical Allele Identifier: CA2733192948
Gene: ALOX12B HGNC NCBI

Linked Data

dbSNP Id: rs2151824739

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8085681A>C , CM000679.2:g.8085681A>C GRCh38
NC_000017.10:g.7988999A>C , CM000679.1:g.7988999A>C GRCh37
NC_000017.9:g.7929724A>C NCBI36
NG_007099.1:g.7023T>G
NG_007099.2:g.7036T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.352+335T>G MANE Select ENSP00000497784.1:n.352+335T>G
ENST00000319144.4:c.352+335T>G ENSP00000315167.4:n.352+335T>G
NM_001139.2:c.352+335T>G NP_001130.1:n.352+335T>G
NM_001139.3:c.352+335T>G MANE Select NP_001130.1:n.352+335T>G