Canonical Allele Identifier: CA2003791837
Gene: HMBS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119092520C= , CM000673.2:g.119092520C= GRCh38
NC_000011.9:g.118963230C= , CM000673.1:g.118963230C= GRCh37
NC_000011.8:g.118468440C= NCBI36
NG_008093.1:g.12644C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000686218.1:c.603C= ENSP00000509288.1:p.His201=
ENST00000691144.1:n.2749C=
ENST00000691249.1:n.1592C=
ENST00000442944.7:c.750C= ENSP00000392041.3:p.His250=
ENST00000640813.1:c.*5C= ENSP00000491061.1:n.*5C=
ENST00000648026.1:c.662C= ENSP00000498044.1:n.662C=
ENST00000648374.1:c.717C= ENSP00000497255.1:p.His239=
ENST00000649823.1:n.1225C=
ENST00000650101.1:c.699C= ENSP00000496970.1:p.His233=
ENST00000650307.1:n.1594C=
ENST00000652429.1:c.768C= MANE Select ENSP00000498786.1:p.His256=
ENST00000278715.7:c.768C= ENSP00000278715.3:p.His256=
ENST00000392841.1:c.717C= ENSP00000376584.1:p.His239=
ENST00000442944.6:c.717C= ENSP00000392041.2:p.His239=
ENST00000537841.5:c.717C= ENSP00000444730.1:p.His239=
ENST00000542044.5:n.1213C=
ENST00000542729.5:c.601-238C= ENSP00000443058.1:n.601-238C=
ENST00000543090.5:c.675C= ENSP00000445429.1:p.His225=
ENST00000543543.5:n.1243C=
ENST00000544182.1:n.983C=
ENST00000544387.5:c.652-238C= ENSP00000438424.1:n.652-238C=
ENST00000546226.5:n.1296C=
NM_000190.3:c.768C= NP_000181.2:p.His256=
NM_001024382.1:c.717C= NP_001019553.1:p.His239=
NM_001258208.1:c.652-238C= NP_001245137.1:n.652-238C=
NM_001258209.1:c.601-238C= NP_001245138.1:n.601-238C=
XM_005271531.1:c.717C= XP_005271588.1:p.His239=
XM_005271532.1:c.717C= XP_005271589.1:p.His239=
XM_005271533.2:c.714C= XP_005271590.1:p.His238=
XM_011542796.1:c.603C= XP_011541098.1:p.His201=
NM_000190.4:c.768C= MANE Select NP_000181.2:p.His256=
NM_001024382.2:c.717C= NP_001019553.1:p.His239=
XM_005271533.3:c.714C= XP_005271590.1:p.His238=
XM_017017629.1:c.717C= XP_016873118.1:p.His239=
XM_024448460.1:c.598-238C= XP_024304228.1:n.598-238C=
NM_001258208.2:c.652-238C= NP_001245137.1:n.652-238C=
NM_001258209.2:c.601-238C= NP_001245138.1:n.601-238C=