Canonical Allele Identifier: CA14959031
Gene: HMOX1 HGNC NCBI

Linked Data

dbSNP Id: rs2071746

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