Canonical Allele Identifier: CA2003791340
Gene: HMBS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119092353C= , CM000673.2:g.119092353C= GRCh38
NC_000011.9:g.118963063C= , CM000673.1:g.118963063C= GRCh37
NC_000011.8:g.118468273C= NCBI36
NG_008093.1:g.12477C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000686218.1:c.487-51C= ENSP00000509288.1:n.487-51C=
ENST00000691144.1:n.2582C=
ENST00000691249.1:n.1425C=
ENST00000442944.7:c.634-51C= ENSP00000392041.3:n.634-51C=
ENST00000536813.6:c.601-51C= ENSP00000438726.2:n.601-51C=
ENST00000640813.1:c.462-51C= ENSP00000491061.1:n.462-51C=
ENST00000648026.1:c.546-51C= ENSP00000498044.1:n.546-51C=
ENST00000648374.1:c.601-51C= ENSP00000497255.1:n.601-51C=
ENST00000649823.1:n.1058C=
ENST00000650101.1:c.583-51C= ENSP00000496970.1:n.583-51C=
ENST00000650307.1:n.1478-51C=
ENST00000652429.1:c.652-51C= MANE Select ENSP00000498786.1:n.652-51C=
ENST00000278715.7:c.652-51C= ENSP00000278715.3:n.652-51C=
ENST00000392841.1:c.601-51C= ENSP00000376584.1:n.601-51C=
ENST00000442944.6:c.601-51C= ENSP00000392041.2:n.601-51C=
ENST00000537841.5:c.601-51C= ENSP00000444730.1:n.601-51C=
ENST00000542044.5:n.1097-51C=
ENST00000542729.5:c.600+190C= ENSP00000443058.1:n.600+190C=
ENST00000543090.5:c.559-51C= ENSP00000445429.1:n.559-51C=
ENST00000543543.5:n.1076C=
ENST00000544182.1:n.816C=
ENST00000544387.5:c.651+190C= ENSP00000438424.1:n.651+190C=
ENST00000545621.5:c.*736C= ENSP00000444849.1:n.*736C=
ENST00000546226.5:n.1129C=
NM_000190.3:c.652-51C= NP_000181.2:n.652-51C=
NM_001024382.1:c.601-51C= NP_001019553.1:n.601-51C=
NM_001258208.1:c.651+190C= NP_001245137.1:n.651+190C=
NM_001258209.1:c.600+190C= NP_001245138.1:n.600+190C=
XM_005271531.1:c.601-51C= XP_005271588.1:n.601-51C=
XM_005271532.1:c.601-51C= XP_005271589.1:n.601-51C=
XM_005271533.2:c.598-51C= XP_005271590.1:n.598-51C=
XM_011542796.1:c.487-51C= XP_011541098.1:n.487-51C=
NM_000190.4:c.652-51C= MANE Select NP_000181.2:n.652-51C=
NM_001024382.2:c.601-51C= NP_001019553.1:n.601-51C=
XM_005271533.3:c.598-51C= XP_005271590.1:n.598-51C=
XM_017017629.1:c.601-51C= XP_016873118.1:n.601-51C=
XM_024448460.1:c.597+190C= XP_024304228.1:n.597+190C=
NM_001258208.2:c.651+190C= NP_001245137.1:n.651+190C=
NM_001258209.2:c.600+190C= NP_001245138.1:n.600+190C=