Canonical Allele Identifier: CA2403372960
Gene: HMOX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.35381625G>T , CM000684.2:g.35381625G>T GRCh38
NC_000022.10:g.35777618G>T , CM000684.1:g.35777618G>T GRCh37
NC_000022.9:g.34107618G>T NCBI36
NG_023030.1:g.5559G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000216117.9:c.23+429G>T MANE Select ENSP00000216117.8:n.23+429G>T
ENST00000481190.2:c.156+296G>T ENSP00000503987.1:n.156+296G>T
ENST00000677931.1:c.23+429G>T ENSP00000502849.1:n.23+429G>T
ENST00000679074.1:c.23+429G>T ENSP00000503459.1:n.23+429G>T
ENST00000216117.8:c.23+429G>T ENSP00000216117.8:n.23+429G>T
ENST00000412893.5:c.23+429G>T ENSP00000413316.1:n.23+429G>T
ENST00000481190.1:n.237+296G>T
NM_002133.2:c.23+429G>T NP_002124.1:n.23+429G>T
NM_002133.3:c.23+429G>T MANE Select NP_002124.1:n.23+429G>T