Canonical Allele Identifier: CA2808396419
Gene: ALOX12B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086291C>G , CM000679.2:g.8086291C>G GRCh38
NC_000017.10:g.7989609C>G , CM000679.1:g.7989609C>G GRCh37
NC_000017.9:g.7930334C>G NCBI36
NG_007099.1:g.6413G>C
NG_007099.2:g.6426G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.148-71G>C MANE Select ENSP00000497784.1:n.148-71G>C
ENST00000319144.4:c.148-71G>C ENSP00000315167.4:n.148-71G>C
NM_001139.2:c.148-71G>C NP_001130.1:n.148-71G>C
NM_001139.3:c.148-71G>C MANE Select NP_001130.1:n.148-71G>C
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