Canonical Allele Identifier: CA398000155
Gene: ALOX12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7989529A>C (hg19) chr17:g.8086211A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086211A>C , CM000679.2:g.8086211A>C GRCh38
NC_000017.10:g.7989529A>C , CM000679.1:g.7989529A>C GRCh37
NC_000017.9:g.7930254A>C NCBI36
NG_007099.1:g.6493T>G
NG_007099.2:g.6506T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.157T>G MANE Select ENSP00000497784.1:p.Tyr53Asp
ENST00000319144.4:c.157T>G ENSP00000315167.4:p.Tyr53Asp
NM_001139.2:c.157T>G NP_001130.1:p.Tyr53Asp
NM_001139.3:c.157T>G MANE Select NP_001130.1:p.Tyr53Asp
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Search 100 bp 3'