Canonical Allele Identifier: CA775590226
Gene: ALOX12B HGNC NCBI

Linked Data

dbSNP Id: rs1203717263
gnomAD v3: 17-8085934-G-A
gnomAD v4: 17-8085934-G-A
MyVariant Identifiers: chr17:g.7989252G>A (hg19) chr17:g.8085934G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8085934G>A , CM000679.2:g.8085934G>A GRCh38
NC_000017.10:g.7989252G>A , CM000679.1:g.7989252G>A GRCh37
NC_000017.9:g.7929977G>A NCBI36
NG_007099.1:g.6770C>T
NG_007099.2:g.6783C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.352+82C>T MANE Select ENSP00000497784.1:n.352+82C>T
ENST00000319144.4:c.352+82C>T ENSP00000315167.4:n.352+82C>T
NM_001139.2:c.352+82C>T NP_001130.1:n.352+82C>T
NM_001139.3:c.352+82C>T MANE Select NP_001130.1:n.352+82C>T
Search 100 bp 5'
Search 100 bp 3'