Canonical Allele Identifier: CA10204705
Gene: HMOX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.35386900G>C , CM000684.2:g.35386900G>C GRCh38
NC_000022.10:g.35782893G>C , CM000684.1:g.35782893G>C GRCh37
NC_000022.9:g.34112893G>C NCBI36
NG_023030.1:g.10834G>C

Transcript Alleles

HGVS Amino-acid Change
NM_002133.3:c.360G>C MANE Select NP_002124.1:p.Glu120Asp
ENST00000216117.9:c.360G>C MANE Select ENSP00000216117.8:p.Glu120Asp
NM_002133.2:c.360G>C NP_002124.1:p.Glu120Asp
ENST00000216117.8:c.360G>C ENSP00000216117.8:p.Glu120Asp
ENST00000412893.5:c.360G>C ENSP00000413316.1:p.Glu120Asp
ENST00000481190.1:n.574G>C
ENST00000481190.2:c.*265G>C ENSP00000503987.1:n.*265G>C
ENST00000677931.1:c.145-2964G>C ENSP00000502849.1:n.145-2964G>C
ENST00000678411.1:c.43-76G>C ENSP00000503526.1:n.43-76G>C
ENST00000679074.1:c.360G>C ENSP00000503459.1:p.Glu120Asp