Canonical Allele Identifier: CA2003780772
Gene: HMBS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119085344C= , CM000673.2:g.119085344C= GRCh38
NC_000011.9:g.118956054C= , CM000673.1:g.118956054C= GRCh37
NC_000011.8:g.118461264C= NCBI36
NG_008093.1:g.5468C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000686218.1:c.-628C= ENSP00000509288.1:n.-628C=
ENST00000691249.1:n.122C=
ENST00000442944.7:c.33+278C= ENSP00000392041.3:n.33+278C=
ENST00000534956.2:n.36+278C=
ENST00000536813.6:c.-102+278C= ENSP00000438726.2:n.-102+278C=
ENST00000546302.6:c.33+278C= ENSP00000445599.1:n.33+278C=
ENST00000640813.1:c.-19+278C= ENSP00000491061.1:n.-19+278C=
ENST00000648026.1:c.27+278C= ENSP00000498044.1:n.27+278C=
ENST00000649823.1:n.55C=
ENST00000649868.1:c.33+278C= ENSP00000497548.1:n.33+278C=
ENST00000650101.1:c.-568C= ENSP00000496970.1:n.-568C=
ENST00000650307.1:n.101C=
ENST00000652429.1:c.33+278C= MANE Select ENSP00000498786.1:n.33+278C=
ENST00000278715.7:c.33+278C= ENSP00000278715.3:n.33+278C=
ENST00000442944.6:c.-102+278C= ENSP00000392041.2:n.-102+278C=
ENST00000535793.5:c.33+278C= ENSP00000439904.1:n.33+278C=
ENST00000536185.5:n.201+278C=
ENST00000536813.5:c.33+278C= ENSP00000438726.1:n.33+278C=
ENST00000537841.5:c.-19+187C= ENSP00000444730.1:n.-19+187C=
ENST00000542044.5:n.158+278C=
ENST00000542729.5:c.-19+187C= ENSP00000443058.1:n.-19+187C=
ENST00000542822.5:c.124+187C= ENSP00000444817.1:n.124+187C=
ENST00000543090.5:c.33+278C= ENSP00000445429.1:n.33+278C=
ENST00000543821.5:n.179+278C=
ENST00000544387.5:c.33+278C= ENSP00000438424.1:n.33+278C=
ENST00000545621.5:c.33+278C= ENSP00000444849.1:n.33+278C=
ENST00000545901.5:n.186+278C=
ENST00000546302.5:c.33+278C= ENSP00000445599.1:n.33+278C=
NM_000190.3:c.33+278C= NP_000181.2:n.33+278C=
NM_001258208.1:c.33+278C= NP_001245137.1:n.33+278C=
NM_001258209.1:c.-19+187C= NP_001245138.1:n.-19+187C=
XM_005271531.1:c.-19+187C= XP_005271588.1:n.-19+187C=
XM_005271532.1:c.-19+211C= XP_005271589.1:n.-19+211C=
XM_005271533.2:c.33+278C= XP_005271590.1:n.33+278C=
NM_000190.4:c.33+278C= MANE Select NP_000181.2:n.33+278C=
XM_005271533.3:c.33+278C= XP_005271590.1:n.33+278C=
XM_024448460.1:c.33+278C= XP_024304228.1:n.33+278C=
NM_001258208.2:c.33+278C= NP_001245137.1:n.33+278C=
NM_001258209.2:c.-19+187C= NP_001245138.1:n.-19+187C=