Canonical Allele Identifier: CA398000018
Gene: ALOX12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7989505G>T (hg19) chr17:g.8086187G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086187G>T , CM000679.2:g.8086187G>T GRCh38
NC_000017.10:g.7989505G>T , CM000679.1:g.7989505G>T GRCh37
NC_000017.9:g.7930230G>T NCBI36
NG_007099.1:g.6517C>A
NG_007099.2:g.6530C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.181C>A MANE Select ENSP00000497784.1:p.Leu61Met
ENST00000319144.4:c.181C>A ENSP00000315167.4:p.Leu61Met
NM_001139.2:c.181C>A NP_001130.1:p.Leu61Met
NM_001139.3:c.181C>A MANE Select NP_001130.1:p.Leu61Met
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