Canonical Allele Identifier: CA775580638
Gene: ALOX12B HGNC NCBI

Linked Data

dbSNP Id: rs1171447348
gnomAD v3: 17-8075384-G-A
gnomAD v4: 17-8075384-G-A
MyVariant Identifiers: chr17:g.7978702G>A (hg19) chr17:g.8075384G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8075384G>A , CM000679.2:g.8075384G>A GRCh38
NC_000017.10:g.7978702G>A , CM000679.1:g.7978702G>A GRCh37
NC_000017.9:g.7919427G>A NCBI36
NG_007099.1:g.17320C>T
NG_007099.2:g.17333C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1654+211C>T MANE Select ENSP00000497784.1:n.1654+211C>T
ENST00000649809.1:c.718+211C>T ENSP00000496845.1:n.718+211C>T
ENST00000319144.4:c.1654+211C>T ENSP00000315167.4:n.1654+211C>T
ENST00000577351.5:n.479+791C>T
NM_001139.2:c.1654+211C>T NP_001130.1:n.1654+211C>T
NM_001139.3:c.1654+211C>T MANE Select NP_001130.1:n.1654+211C>T
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