Canonical Allele Identifier: CA973984702
Gene: HMOX2 HGNC NCBI

Linked Data

dbSNP Id: rs2058807450

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4510328_4510329insTT , CM000678.2:g.4510328_4510329insTT GRCh38
NC_000016.9:g.4560329_4560330insTT , CM000678.1:g.4560329_4560330insTT GRCh37
NC_000016.8:g.4500330_4500331insTT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000570646.6:c.*572_*573insTT MANE Select ENSP00000459214.1:n.*572_*573insTT
ENST00000219700.10:c.*572_*573insTT ENSP00000219700.6:n.*572_*573insTT
ENST00000406590.6:c.*572_*573insTT ENSP00000385100.2:n.*572_*573insTT
ENST00000414777.5:c.*572_*573insTT ENSP00000391637.1:n.*572_*573insTT
ENST00000570646.5:c.*572_*573insTT ENSP00000459214.1:n.*572_*573insTT
ENST00000613539.1:c.1685_1686insTT ENSP00000477572.1:n.1685_1686insTT
ENST00000619528.4:c.*572_*573insTT ENSP00000484423.1:n.*572_*573insTT
ENST00000619913.4:c.*572_*573insTT ENSP00000484467.1:n.*572_*573insTT
NM_001127204.1:c.*572_*573insTT NP_001120676.1:n.*572_*573insTT
NM_001127205.1:c.*572_*573insTT NP_001120677.1:n.*572_*573insTT
NM_001127206.2:c.*572_*573insTT NP_001120678.1:n.*572_*573insTT
NM_001286267.1:c.*572_*573insTT NP_001273196.1:n.*572_*573insTT
NM_001286268.1:c.*572_*573insTT NP_001273197.1:n.*572_*573insTT
NM_001286269.1:c.*572_*573insTT NP_001273198.1:n.*572_*573insTT
NM_001286270.1:c.*572_*573insTT NP_001273199.1:n.*572_*573insTT
NM_001286271.1:c.*572_*573insTT NP_001273200.1:n.*572_*573insTT
NM_002134.3:c.*572_*573insTT NP_002125.3:n.*572_*573insTT
XM_011522473.1:c.*572_*573insTT XP_011520775.1:n.*572_*573insTT
XM_017023197.2:c.*572_*573insTT XP_016878686.1:n.*572_*573insTT
XM_024450250.1:c.*572_*573insTT XP_024306018.1:n.*572_*573insTT
NM_002134.4:c.*572_*573insTT MANE Select NP_002125.3:n.*572_*573insTT
NM_001127204.2:c.*572_*573insTT NP_001120676.1:n.*572_*573insTT
NM_001127205.2:c.*572_*573insTT NP_001120677.1:n.*572_*573insTT
NM_001127206.3:c.*572_*573insTT NP_001120678.1:n.*572_*573insTT
NM_001286267.2:c.*572_*573insTT NP_001273196.1:n.*572_*573insTT
NM_001286268.2:c.*572_*573insTT NP_001273197.1:n.*572_*573insTT
NM_001286269.2:c.*572_*573insTT NP_001273198.1:n.*572_*573insTT
NM_001286270.2:c.*572_*573insTT NP_001273199.1:n.*572_*573insTT
NM_001286271.2:c.*572_*573insTT NP_001273200.1:n.*572_*573insTT