Canonical Allele Identifier: CA10204669

Gene: HMOX1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35386793C>T , CM000684.2:g.35386793C>T	GRCh38
NC_000022.10:g.35782786C>T , CM000684.1:g.35782786C>T	GRCh37
NC_000022.9:g.34112786C>T	NCBI36
NG_023030.1:g.10727C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216117.9:c.253C>T MANE Select	ENSP00000216117.8:p.Arg85Cys
ENST00000481190.2:c.*158C>T	ENSP00000503987.1:n.*158C>T
ENST00000677931.1:c.145-3071C>T	ENSP00000502849.1:n.145-3071C>T
ENST00000678411.1:c.43-183C>T	ENSP00000503526.1:n.43-183C>T
ENST00000679074.1:c.253C>T	ENSP00000503459.1:p.Arg85Cys
ENST00000216117.8:c.253C>T	ENSP00000216117.8:p.Arg85Cys
ENST00000412893.5:c.253C>T	ENSP00000413316.1:p.Arg85Cys
ENST00000481190.1:n.467C>T
NM_002133.2:c.253C>T	NP_002124.1:p.Arg85Cys
NM_002133.3:c.253C>T MANE Select	NP_002124.1:p.Arg85Cys