Canonical Allele Identifier: CA382898388

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.118963499A>G (hg19) ; chr11:g.119092789A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092789A>G , CM000673.2:g.119092789A>G	GRCh38
NC_000011.9:g.118963499A>G , CM000673.1:g.118963499A>G	GRCh37
NC_000011.8:g.118468709A>G	NCBI36
NG_008093.1:g.12913A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.638A>G	ENSP00000509288.1:p.His213Arg
ENST00000691144.1:n.3018A>G
ENST00000691249.1:n.1627A>G
ENST00000442944.7:c.785A>G	ENSP00000392041.3:p.His262Arg
ENST00000640813.1:c.*40A>G	ENSP00000491061.1:n.*40A>G
ENST00000648026.1:c.697A>G	ENSP00000498044.1:n.697A>G
ENST00000648374.1:c.752A>G	ENSP00000497255.1:p.His251Arg
ENST00000649823.1:n.1260A>G
ENST00000650101.1:c.734A>G	ENSP00000496970.1:p.His245Arg
ENST00000650307.1:n.1629A>G
ENST00000652429.1:c.803A>G MANE Select	ENSP00000498786.1:p.His268Arg
ENST00000278715.7:c.803A>G	ENSP00000278715.3:p.His268Arg
ENST00000392841.1:c.752A>G	ENSP00000376584.1:p.His251Arg
ENST00000442944.6:c.752A>G	ENSP00000392041.2:p.His251Arg
ENST00000537841.5:c.752A>G	ENSP00000444730.1:p.His251Arg
ENST00000539045.1:n.179A>G
ENST00000542044.5:n.1248A>G
ENST00000542729.5:c.632A>G	ENSP00000443058.1:p.His211Arg
ENST00000543090.5:c.710A>G	ENSP00000445429.1:p.His237Arg
ENST00000543543.5:n.1278A>G
ENST00000544182.1:n.1252A>G
ENST00000544387.5:c.683A>G	ENSP00000438424.1:p.His228Arg
ENST00000546226.5:n.1565A>G
NM_000190.3:c.803A>G	NP_000181.2:p.His268Arg
NM_001024382.1:c.752A>G	NP_001019553.1:p.His251Arg
NM_001258208.1:c.683A>G	NP_001245137.1:p.His228Arg
NM_001258209.1:c.632A>G	NP_001245138.1:p.His211Arg
XM_005271531.1:c.752A>G	XP_005271588.1:p.His251Arg
XM_005271532.1:c.752A>G	XP_005271589.1:p.His251Arg
XM_005271533.2:c.749A>G	XP_005271590.1:p.His250Arg
XM_011542796.1:c.638A>G	XP_011541098.1:p.His213Arg
NM_000190.4:c.803A>G MANE Select	NP_000181.2:p.His268Arg
NM_001024382.2:c.752A>G	NP_001019553.1:p.His251Arg
XM_005271533.3:c.749A>G	XP_005271590.1:p.His250Arg
XM_017017629.1:c.752A>G	XP_016873118.1:p.His251Arg
XM_024448460.1:c.629A>G	XP_024304228.1:p.His210Arg
NM_001258208.2:c.683A>G	NP_001245137.1:p.His228Arg
NM_001258209.2:c.632A>G	NP_001245138.1:p.His211Arg