Canonical Allele Identifier: CA398000133
Gene: ALOX12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7989525G>C (hg19) chr17:g.8086207G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086207G>C , CM000679.2:g.8086207G>C GRCh38
NC_000017.10:g.7989525G>C , CM000679.1:g.7989525G>C GRCh37
NC_000017.9:g.7930250G>C NCBI36
NG_007099.1:g.6497C>G
NG_007099.2:g.6510C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.161C>G MANE Select ENSP00000497784.1:p.Thr54Ser
ENST00000319144.4:c.161C>G ENSP00000315167.4:p.Thr54Ser
NM_001139.2:c.161C>G NP_001130.1:p.Thr54Ser
NM_001139.3:c.161C>G MANE Select NP_001130.1:p.Thr54Ser
Search 100 bp 5'
Search 100 bp 3'