Canonical Allele Identifier: CA14959031

Gene: HMOX1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35380679A>T , CM000684.2:g.35380679A>T	GRCh38
NC_000022.10:g.35776672A>T , CM000684.1:g.35776672A>T	GRCh37
NC_000022.9:g.34106672A>T	NCBI36
NG_023030.1:g.4613A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412893.5:c.-241+199A>T	ENSP00000413316.1:n.-241+199A>T