Canonical Allele Identifier: CA2003791693
Gene: HMBS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119092488C= , CM000673.2:g.119092488C= GRCh38
NC_000011.9:g.118963198C= , CM000673.1:g.118963198C= GRCh37
NC_000011.8:g.118468408C= NCBI36
NG_008093.1:g.12612C=

Transcript Alleles

HGVS Amino-acid change
ENST00000686218.1:c.571C= ENSP00000509288.1:p.Arg191=
ENST00000691144.1:n.2717C=
ENST00000691249.1:n.1560C=
ENST00000442944.7:c.718C= ENSP00000392041.3:p.Arg240=
ENST00000640813.1:c.546C= ENSP00000491061.1:p.Phe182=
ENST00000648026.1:c.630C= ENSP00000498044.1:p.Phe210=
ENST00000648374.1:c.685C= ENSP00000497255.1:p.Arg229=
ENST00000649823.1:n.1193C=
ENST00000650101.1:c.667C= ENSP00000496970.1:p.Arg223=
ENST00000650307.1:n.1562C=
ENST00000652429.1:c.736C= MANE Select ENSP00000498786.1:p.Arg246=
ENST00000278715.7:c.736C= ENSP00000278715.3:p.Arg246=
ENST00000392841.1:c.685C= ENSP00000376584.1:p.Arg229=
ENST00000442944.6:c.685C= ENSP00000392041.2:p.Arg229=
ENST00000537841.5:c.685C= ENSP00000444730.1:p.Arg229=
ENST00000542044.5:n.1181C=
ENST00000542729.5:c.601-270C= ENSP00000443058.1:n.601-270C=
ENST00000543090.5:c.643C= ENSP00000445429.1:p.Arg215=
ENST00000543543.5:n.1211C=
ENST00000544182.1:n.951C=
ENST00000544387.5:c.652-270C= ENSP00000438424.1:n.652-270C=
ENST00000545621.5:c.*871C= ENSP00000444849.1:n.*871C=
ENST00000546226.5:n.1264C=
NM_000190.3:c.736C= NP_000181.2:p.Arg246=
NM_001024382.1:c.685C= NP_001019553.1:p.Arg229=
NM_001258208.1:c.652-270C= NP_001245137.1:n.652-270C=
NM_001258209.1:c.601-270C= NP_001245138.1:n.601-270C=
XM_005271531.1:c.685C= XP_005271588.1:p.Arg229=
XM_005271532.1:c.685C= XP_005271589.1:p.Arg229=
XM_005271533.2:c.682C= XP_005271590.1:p.Arg228=
XM_011542796.1:c.571C= XP_011541098.1:p.Arg191=
NM_000190.4:c.736C= MANE Select NP_000181.2:p.Arg246=
NM_001024382.2:c.685C= NP_001019553.1:p.Arg229=
XM_005271533.3:c.682C= XP_005271590.1:p.Arg228=
XM_017017629.1:c.685C= XP_016873118.1:p.Arg229=
XM_024448460.1:c.598-270C= XP_024304228.1:n.598-270C=
NM_001258208.2:c.652-270C= NP_001245137.1:n.652-270C=
NM_001258209.2:c.601-270C= NP_001245138.1:n.601-270C=