Canonical Allele Identifier: CA2003780781
Gene: HMBS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119085353C= , CM000673.2:g.119085353C= GRCh38
NC_000011.9:g.118956063C= , CM000673.1:g.118956063C= GRCh37
NC_000011.8:g.118461273C= NCBI36
NG_008093.1:g.5477C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000686218.1:c.-619C= ENSP00000509288.1:n.-619C=
ENST00000691249.1:n.131C=
ENST00000442944.7:c.33+287C= ENSP00000392041.3:n.33+287C=
ENST00000534956.2:n.36+287C=
ENST00000536813.6:c.-102+287C= ENSP00000438726.2:n.-102+287C=
ENST00000546302.6:c.33+287C= ENSP00000445599.1:n.33+287C=
ENST00000640813.1:c.-19+287C= ENSP00000491061.1:n.-19+287C=
ENST00000648026.1:c.27+287C= ENSP00000498044.1:n.27+287C=
ENST00000649823.1:n.64C=
ENST00000649868.1:c.33+287C= ENSP00000497548.1:n.33+287C=
ENST00000650101.1:c.-559C= ENSP00000496970.1:n.-559C=
ENST00000650307.1:n.110C=
ENST00000652429.1:c.33+287C= MANE Select ENSP00000498786.1:n.33+287C=
ENST00000278715.7:c.33+287C= ENSP00000278715.3:n.33+287C=
ENST00000442944.6:c.-102+287C= ENSP00000392041.2:n.-102+287C=
ENST00000535793.5:c.33+287C= ENSP00000439904.1:n.33+287C=
ENST00000536185.5:n.201+287C=
ENST00000536813.5:c.33+287C= ENSP00000438726.1:n.33+287C=
ENST00000537841.5:c.-19+196C= ENSP00000444730.1:n.-19+196C=
ENST00000542044.5:n.158+287C=
ENST00000542729.5:c.-19+196C= ENSP00000443058.1:n.-19+196C=
ENST00000542822.5:c.124+196C= ENSP00000444817.1:n.124+196C=
ENST00000543090.5:c.33+287C= ENSP00000445429.1:n.33+287C=
ENST00000543821.5:n.179+287C=
ENST00000544387.5:c.33+287C= ENSP00000438424.1:n.33+287C=
ENST00000545621.5:c.33+287C= ENSP00000444849.1:n.33+287C=
ENST00000545901.5:n.186+287C=
ENST00000546302.5:c.33+287C= ENSP00000445599.1:n.33+287C=
NM_000190.3:c.33+287C= NP_000181.2:n.33+287C=
NM_001258208.1:c.33+287C= NP_001245137.1:n.33+287C=
NM_001258209.1:c.-19+196C= NP_001245138.1:n.-19+196C=
XM_005271531.1:c.-19+196C= XP_005271588.1:n.-19+196C=
XM_005271532.1:c.-19+220C= XP_005271589.1:n.-19+220C=
XM_005271533.2:c.33+287C= XP_005271590.1:n.33+287C=
NM_000190.4:c.33+287C= MANE Select NP_000181.2:n.33+287C=
XM_005271533.3:c.33+287C= XP_005271590.1:n.33+287C=
XM_024448460.1:c.33+287C= XP_024304228.1:n.33+287C=
NM_001258208.2:c.33+287C= NP_001245137.1:n.33+287C=
NM_001258209.2:c.-19+196C= NP_001245138.1:n.-19+196C=