Canonical Allele Identifier: CA2246104956
Gene: ALOX12B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086226C= , CM000679.2:g.8086226C= GRCh38
NC_000017.10:g.7989544C= , CM000679.1:g.7989544C= GRCh37
NC_000017.9:g.7930269C= NCBI36
NG_007099.1:g.6478G=
NG_007099.2:g.6491G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.148-6G= MANE Select ENSP00000497784.1:n.148-6G=
ENST00000319144.4:c.148-6G= ENSP00000315167.4:n.148-6G=
NM_001139.2:c.148-6G= NP_001130.1:n.148-6G=
NM_001139.3:c.148-6G= MANE Select NP_001130.1:n.148-6G=
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