Canonical Allele Identifier: CA397989807
Gene: ALOX12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7978963G>C (hg19) chr17:g.8075645G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8075645G>C , CM000679.2:g.8075645G>C GRCh38
NC_000017.10:g.7978963G>C , CM000679.1:g.7978963G>C GRCh37
NC_000017.9:g.7919688G>C NCBI36
NG_007099.1:g.17059C>G
NG_007099.2:g.17072C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1604C>G MANE Select ENSP00000497784.1:p.Ser535Cys
ENST00000649809.1:c.668C>G ENSP00000496845.1:p.Ser223Cys
ENST00000319144.4:c.1604C>G ENSP00000315167.4:p.Ser535Cys
ENST00000577351.5:n.479+530C>G
NM_001139.2:c.1604C>G NP_001130.1:p.Ser535Cys
NM_001139.3:c.1604C>G MANE Select NP_001130.1:p.Ser535Cys
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