Canonical Allele Identifier: CA14342077
Gene: HMOX2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1051308

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4510300G>A , CM000678.2:g.4510300G>A GRCh38
NC_000016.9:g.4560301G>A , CM000678.1:g.4560301G>A GRCh37
NC_000016.8:g.4500302G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001127204.1:c.*544G>A VV NP_001120676.1:p.=
NM_001127205.1:c.*544G>A VV NP_001120677.1:p.=
NM_001127206.2:c.*544G>A VV NP_001120678.1:p.=
NM_001286267.1:c.*544G>A VV NP_001273196.1:p.=
NM_001286268.1:c.*544G>A VV NP_001273197.1:p.=
NM_001286269.1:c.*544G>A VV NP_001273198.1:p.=
NM_001286270.1:c.*544G>A VV NP_001273199.1:p.=
NM_001286271.1:c.*544G>A VV NP_001273200.1:p.=
NM_002134.3:c.*544G>A VV NP_002125.3:p.=
XM_011522473.1:c.*544G>A XP_011520775.1:p.=
XM_017023197.2:c.*544G>A XP_016878686.1:p.=
XM_024450250.1:c.*544G>A XP_024306018.1:p.=
ENST00000219700.10:c.*544G>A ENSP00000219700.6:p.=
ENST00000406590.6:c.*544G>A ENSP00000385100.2:p.=
ENST00000414777.5:c.*544G>A ENSP00000391637.1:p.=
ENST00000570646.5:c.*544G>A ENSP00000459214.1:p.=
ENST00000613539.1:n.1657G>A ENSP00000477572.1:p.=
ENST00000619528.4:c.*544G>A ENSP00000484423.1:p.=
ENST00000619913.4:c.*544G>A ENSP00000484467.1:p.=