Canonical Allele Identifier: CA2003791470
Gene: HMBS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119092414G= , CM000673.2:g.119092414G= GRCh38
NC_000011.9:g.118963124G= , CM000673.1:g.118963124G= GRCh37
NC_000011.8:g.118468334G= NCBI36
NG_008093.1:g.12538G=

Transcript Alleles

HGVS Amino-acid change
ENST00000686218.1:c.497G= ENSP00000509288.1:p.Gly166=
ENST00000691144.1:n.2643G=
ENST00000691249.1:n.1486G=
ENST00000442944.7:c.644G= ENSP00000392041.3:p.Gly215=
ENST00000536813.6:c.611G= ENSP00000438726.2:p.Gly204=
ENST00000640813.1:c.472G= ENSP00000491061.1:p.Ala158=
ENST00000648026.1:c.556G= ENSP00000498044.1:p.Ala186=
ENST00000648374.1:c.611G= ENSP00000497255.1:p.Gly204=
ENST00000649823.1:n.1119G=
ENST00000650101.1:c.593G= ENSP00000496970.1:p.Gly198=
ENST00000650307.1:n.1488G=
ENST00000652429.1:c.662G= MANE Select ENSP00000498786.1:p.Gly221=
ENST00000278715.7:c.662G= ENSP00000278715.3:p.Gly221=
ENST00000392841.1:c.611G= ENSP00000376584.1:p.Gly204=
ENST00000442944.6:c.611G= ENSP00000392041.2:p.Gly204=
ENST00000537841.5:c.611G= ENSP00000444730.1:p.Gly204=
ENST00000542044.5:n.1107G=
ENST00000542729.5:c.600+251G= ENSP00000443058.1:n.600+251G=
ENST00000543090.5:c.569G= ENSP00000445429.1:p.Gly190=
ENST00000543543.5:n.1137G=
ENST00000544182.1:n.877G=
ENST00000544387.5:c.651+251G= ENSP00000438424.1:n.651+251G=
ENST00000545621.5:c.*797G= ENSP00000444849.1:n.*797G=
ENST00000546226.5:n.1190G=
NM_000190.3:c.662G= NP_000181.2:p.Gly221=
NM_001024382.1:c.611G= NP_001019553.1:p.Gly204=
NM_001258208.1:c.651+251G= NP_001245137.1:n.651+251G=
NM_001258209.1:c.600+251G= NP_001245138.1:n.600+251G=
XM_005271531.1:c.611G= XP_005271588.1:p.Gly204=
XM_005271532.1:c.611G= XP_005271589.1:p.Gly204=
XM_005271533.2:c.608G= XP_005271590.1:p.Gly203=
XM_011542796.1:c.497G= XP_011541098.1:p.Gly166=
NM_000190.4:c.662G= MANE Select NP_000181.2:p.Gly221=
NM_001024382.2:c.611G= NP_001019553.1:p.Gly204=
XM_005271533.3:c.608G= XP_005271590.1:p.Gly203=
XM_017017629.1:c.611G= XP_016873118.1:p.Gly204=
XM_024448460.1:c.597+251G= XP_024304228.1:n.597+251G=
NM_001258208.2:c.651+251G= NP_001245137.1:n.651+251G=
NM_001258209.2:c.600+251G= NP_001245138.1:n.600+251G=