Canonical Allele Identifier: CA775581991

Gene: ALOX12B

Linked Data

• dbSNP Id: rs1421747863
• gnomAD v3: 17-8076536-C-CTCCCT
• gnomAD v4: 17-8076536-C-CTCCCT
• MyVariant Identifiers: chr17:g.7979854_7979855insTCCCT (hg19) ; chr17:g.8076536_8076537insTCCCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8076537_8076541dup , CM000679.2:g.8076537_8076541dup	GRCh38
NC_000017.10:g.7979855_7979859dup , CM000679.1:g.7979855_7979859dup	GRCh37
NC_000017.9:g.7920580_7920584dup	NCBI36
NG_007099.1:g.16163_16167dup
NG_007099.2:g.16176_16180dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.1362+116_1362+120dup MANE Select	ENSP00000497784.1:n.1362+116_1362+120dup
ENST00000649809.1:c.426+116_426+120dup	ENSP00000496845.1:n.426+116_426+120dup
ENST00000319144.4:c.1362+116_1362+120dup	ENSP00000315167.4:n.1362+116_1362+120dup
ENST00000577351.5:n.309+116_309+120dup
ENST00000583276.5:n.746+116_746+120dup
ENST00000584116.1:n.618+116_618+120dup
NM_001139.2:c.1362+116_1362+120dup	NP_001130.1:n.1362+116_1362+120dup
NM_001139.3:c.1362+116_1362+120dup MANE Select	NP_001130.1:n.1362+116_1362+120dup