Canonical Allele Identifier: CA2003791427
Gene: HMBS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119092406G= , CM000673.2:g.119092406G= GRCh38
NC_000011.9:g.118963116G= , CM000673.1:g.118963116G= GRCh37
NC_000011.8:g.118468326G= NCBI36
NG_008093.1:g.12530G=

Transcript Alleles

HGVS Amino-acid change
ENST00000686218.1:c.489G= ENSP00000509288.1:p.Gly163=
ENST00000691144.1:n.2635G=
ENST00000691249.1:n.1478G=
ENST00000442944.7:c.636G= ENSP00000392041.3:p.Gly212=
ENST00000536813.6:c.603G= ENSP00000438726.2:p.Gly201=
ENST00000640813.1:c.464G= ENSP00000491061.1:p.Gly155=
ENST00000648026.1:c.548G= ENSP00000498044.1:p.Gly183=
ENST00000648374.1:c.603G= ENSP00000497255.1:p.Gly201=
ENST00000649823.1:n.1111G=
ENST00000650101.1:c.585G= ENSP00000496970.1:p.Gly195=
ENST00000650307.1:n.1480G=
ENST00000652429.1:c.654G= MANE Select ENSP00000498786.1:p.Gly218=
ENST00000278715.7:c.654G= ENSP00000278715.3:p.Gly218=
ENST00000392841.1:c.603G= ENSP00000376584.1:p.Gly201=
ENST00000442944.6:c.603G= ENSP00000392041.2:p.Gly201=
ENST00000537841.5:c.603G= ENSP00000444730.1:p.Gly201=
ENST00000542044.5:n.1099G=
ENST00000542729.5:c.600+243G= ENSP00000443058.1:n.600+243G=
ENST00000543090.5:c.561G= ENSP00000445429.1:p.Gly187=
ENST00000543543.5:n.1129G=
ENST00000544182.1:n.869G=
ENST00000544387.5:c.651+243G= ENSP00000438424.1:n.651+243G=
ENST00000545621.5:c.*789G= ENSP00000444849.1:n.*789G=
ENST00000546226.5:n.1182G=
NM_000190.3:c.654G= NP_000181.2:p.Gly218=
NM_001024382.1:c.603G= NP_001019553.1:p.Gly201=
NM_001258208.1:c.651+243G= NP_001245137.1:n.651+243G=
NM_001258209.1:c.600+243G= NP_001245138.1:n.600+243G=
XM_005271531.1:c.603G= XP_005271588.1:p.Gly201=
XM_005271532.1:c.603G= XP_005271589.1:p.Gly201=
XM_005271533.2:c.600G= XP_005271590.1:p.Gly200=
XM_011542796.1:c.489G= XP_011541098.1:p.Gly163=
NM_000190.4:c.654G= MANE Select NP_000181.2:p.Gly218=
NM_001024382.2:c.603G= NP_001019553.1:p.Gly201=
XM_005271533.3:c.600G= XP_005271590.1:p.Gly200=
XM_017017629.1:c.603G= XP_016873118.1:p.Gly201=
XM_024448460.1:c.597+243G= XP_024304228.1:n.597+243G=
NM_001258208.2:c.651+243G= NP_001245137.1:n.651+243G=
NM_001258209.2:c.600+243G= NP_001245138.1:n.600+243G=