Canonical Allele Identifier: CA397989534
Gene: ALOX12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7978930A>T (hg19) chr17:g.8075612A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8075612A>T , CM000679.2:g.8075612A>T GRCh38
NC_000017.10:g.7978930A>T , CM000679.1:g.7978930A>T GRCh37
NC_000017.9:g.7919655A>T NCBI36
NG_007099.1:g.17092T>A
NG_007099.2:g.17105T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647874.1:c.1637T>A MANE Select ENSP00000497784.1:p.Leu546Gln
ENST00000649809.1:c.701T>A ENSP00000496845.1:p.Leu234Gln
ENST00000319144.4:c.1637T>A ENSP00000315167.4:p.Leu546Gln
ENST00000577351.5:n.479+563T>A
NM_001139.2:c.1637T>A NP_001130.1:p.Leu546Gln
NM_001139.3:c.1637T>A MANE Select NP_001130.1:p.Leu546Gln
Search 100 bp 5'
Search 100 bp 3'