Canonical Allele Identifier: CA323526638

Gene: HMOX1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35391174C>T , CM000684.2:g.35391174C>T	GRCh38
NC_000022.10:g.35787167C>T , CM000684.1:g.35787167C>T	GRCh37
NC_000022.9:g.34117167C>T	NCBI36
NG_023030.1:g.15108C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216117.9:c.736+1211C>T MANE Select	ENSP00000216117.8:n.736+1211C>T
ENST00000481190.2:c.*641+1211C>T	ENSP00000503987.1:n.*641+1211C>T
ENST00000677931.1:c.244+1211C>T	ENSP00000502849.1:n.244+1211C>T
ENST00000678411.1:c.343+1211C>T	ENSP00000503526.1:n.343+1211C>T
ENST00000679074.1:c.637-2294C>T	ENSP00000503459.1:n.637-2294C>T
ENST00000216117.8:c.736+1211C>T	ENSP00000216117.8:n.736+1211C>T
NM_002133.2:c.736+1211C>T	NP_002124.1:n.736+1211C>T
NM_002133.3:c.736+1211C>T MANE Select	NP_002124.1:n.736+1211C>T