Canonical Allele Identifier: CA10204718

Gene: HMOX1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35386947G>A , CM000684.2:g.35386947G>A	GRCh38
NC_000022.10:g.35782940G>A , CM000684.1:g.35782940G>A	GRCh37
NC_000022.9:g.34112940G>A	NCBI36
NG_023030.1:g.10881G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002133.3:c.407G>A MANE Select	NP_002124.1:p.Arg136His
ENST00000216117.9:c.407G>A MANE Select	ENSP00000216117.8:p.Arg136His
NM_002133.2:c.407G>A	NP_002124.1:p.Arg136His
ENST00000216117.8:c.407G>A	ENSP00000216117.8:p.Arg136His
ENST00000412893.5:c.407G>A	ENSP00000413316.1:p.Arg136His
ENST00000481190.2:c.*312G>A	ENSP00000503987.1:n.*312G>A
ENST00000677931.1:c.145-2917G>A	ENSP00000502849.1:n.145-2917G>A
ENST00000678411.1:c.43-29G>A	ENSP00000503526.1:n.43-29G>A
ENST00000679074.1:c.407G>A	ENSP00000503459.1:p.Arg136His