Canonical Allele Identifier: CA2003790941
Gene: HMBS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119092159G= , CM000673.2:g.119092159G= GRCh38
NC_000011.9:g.118962869G= , CM000673.1:g.118962869G= GRCh37
NC_000011.8:g.118468079G= NCBI36
NG_008093.1:g.12283G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000686218.1:c.482G= ENSP00000509288.1:p.Gly161=
ENST00000691144.1:n.2388G=
ENST00000691249.1:n.1231G=
ENST00000442944.7:c.629G= ENSP00000392041.3:p.Gly210=
ENST00000536813.6:c.596G= ENSP00000438726.2:p.Gly199=
ENST00000546302.6:c.569G= ENSP00000445599.1:p.Gly190=
ENST00000640813.1:c.462-245G= ENSP00000491061.1:n.462-245G=
ENST00000648026.1:c.541G= ENSP00000498044.1:p.Ala181=
ENST00000648374.1:c.596G= ENSP00000497255.1:p.Gly199=
ENST00000648488.1:c.*120G= ENSP00000498079.1:n.*120G=
ENST00000649823.1:n.864G=
ENST00000650101.1:c.578G= ENSP00000496970.1:p.Gly193=
ENST00000650307.1:n.1473G=
ENST00000652429.1:c.647G= MANE Select ENSP00000498786.1:p.Gly216=
ENST00000278715.7:c.647G= ENSP00000278715.3:p.Gly216=
ENST00000392841.1:c.596G= ENSP00000376584.1:p.Gly199=
ENST00000442944.6:c.596G= ENSP00000392041.2:p.Gly199=
ENST00000537841.5:c.596G= ENSP00000444730.1:p.Gly199=
ENST00000542044.5:n.1092G=
ENST00000542345.5:n.785G=
ENST00000542729.5:c.596G= ENSP00000443058.1:p.Gly199=
ENST00000543090.5:c.559-245G= ENSP00000445429.1:n.559-245G=
ENST00000543543.5:n.882G=
ENST00000544182.1:n.622G=
ENST00000544387.5:c.647G= ENSP00000438424.1:p.Gly216=
ENST00000545621.5:c.*542G= ENSP00000444849.1:n.*542G=
ENST00000546226.5:n.935G=
ENST00000546302.5:c.569G= ENSP00000445599.1:p.Gly190=
NM_000190.3:c.647G= NP_000181.2:p.Gly216=
NM_001024382.1:c.596G= NP_001019553.1:p.Gly199=
NM_001258208.1:c.647G= NP_001245137.1:p.Gly216=
NM_001258209.1:c.596G= NP_001245138.1:p.Gly199=
XM_005271531.1:c.596G= XP_005271588.1:p.Gly199=
XM_005271532.1:c.596G= XP_005271589.1:p.Gly199=
XM_005271533.2:c.593G= XP_005271590.1:p.Gly198=
XM_011542796.1:c.482G= XP_011541098.1:p.Gly161=
NM_000190.4:c.647G= MANE Select NP_000181.2:p.Gly216=
NM_001024382.2:c.596G= NP_001019553.1:p.Gly199=
XM_005271533.3:c.593G= XP_005271590.1:p.Gly198=
XM_017017629.1:c.596G= XP_016873118.1:p.Gly199=
XM_024448460.1:c.593G= XP_024304228.1:p.Gly198=
NM_001258208.2:c.647G= NP_001245137.1:p.Gly216=
NM_001258209.2:c.596G= NP_001245138.1:p.Gly199=