Canonical Allele Identifier: CA2003780501
Gene: HMBS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119084956G= , CM000673.2:g.119084956G= GRCh38
NC_000011.9:g.118955666G= , CM000673.1:g.118955666G= GRCh37
NC_000011.8:g.118460876G= NCBI36
NG_008093.1:g.5080G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000442944.7:c.-78G= ENSP00000392041.3:n.-78G=
ENST00000536813.6:c.-212G= ENSP00000438726.2:n.-212G=
ENST00000546302.6:c.-78G= ENSP00000445599.1:n.-78G=
ENST00000640813.1:c.-129G= ENSP00000491061.1:n.-129G=
ENST00000652429.1:c.-78G= MANE Select ENSP00000498786.1:n.-78G=
ENST00000278715.7:c.-78G= ENSP00000278715.3:n.-78G=
ENST00000442944.6:c.-212G= ENSP00000392041.2:n.-212G=
ENST00000535793.5:c.-78G= ENSP00000439904.1:n.-78G=
ENST00000536185.5:n.91G=
ENST00000536813.5:c.-78G= ENSP00000438726.1:n.-78G=
ENST00000537841.5:c.-220G= ENSP00000444730.1:n.-220G=
ENST00000542044.5:n.48G=
ENST00000542729.5:c.-220G= ENSP00000443058.1:n.-220G=
ENST00000542822.5:c.-78G= ENSP00000444817.1:n.-78G=
ENST00000543090.5:c.-78G= ENSP00000445429.1:n.-78G=
ENST00000543821.5:n.69G=
ENST00000544387.5:c.-78G= ENSP00000438424.1:n.-78G=
ENST00000545621.5:c.-78G= ENSP00000444849.1:n.-78G=
ENST00000545901.5:n.76G=
ENST00000546302.5:c.-78G= ENSP00000445599.1:n.-78G=
NM_000190.3:c.-78G= NP_000181.2:n.-78G=
NM_001258208.1:c.-78G= NP_001245137.1:n.-78G=
NM_001258209.1:c.-220G= NP_001245138.1:n.-220G=
XM_005271531.1:c.-220G= XP_005271588.1:n.-220G=
XM_005271532.1:c.-196G= XP_005271589.1:n.-196G=
XM_005271533.2:c.-78G= XP_005271590.1:n.-78G=
NM_000190.4:c.-78G= MANE Select NP_000181.2:n.-78G=
XM_005271533.3:c.-78G= XP_005271590.1:n.-78G=
XM_024448460.1:c.-78G= XP_024304228.1:n.-78G=
NM_001258208.2:c.-78G= NP_001245137.1:n.-78G=
NM_001258209.2:c.-220G= NP_001245138.1:n.-220G=