Canonical Allele Identifier: CA2403375569
Gene: HMOX1 HGNC NCBI

Linked Data

dbSNP Id: rs2071749
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.35387420A>C , CM000684.2:g.35387420A>C GRCh38
NC_000022.10:g.35783413A>C , CM000684.1:g.35783413A>C GRCh37
NC_000022.9:g.34113413A>C NCBI36
NG_023030.1:g.11354A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000216117.9:c.636+244A>C MANE Select ENSP00000216117.8:n.636+244A>C
ENST00000481190.2:c.*541+244A>C ENSP00000503987.1:n.*541+244A>C
ENST00000677931.1:c.145-2444A>C ENSP00000502849.1:n.145-2444A>C
ENST00000678411.1:c.243+244A>C ENSP00000503526.1:n.243+244A>C
ENST00000679074.1:c.636+244A>C ENSP00000503459.1:n.636+244A>C
ENST00000216117.8:c.636+244A>C ENSP00000216117.8:n.636+244A>C
ENST00000494998.1:n.137+244A>C
NM_002133.2:c.636+244A>C NP_002124.1:n.636+244A>C
NM_002133.3:c.636+244A>C MANE Select NP_002124.1:n.636+244A>C
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