Canonical Allele Identifier: CA2616352594
Gene: HMBS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119085099G>C , CM000673.2:g.119085099G>C GRCh38
NC_000011.9:g.118955809G>C , CM000673.1:g.118955809G>C GRCh37
NC_000011.8:g.118461019G>C NCBI36
NG_008093.1:g.5223G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000442944.7:c.33+33G>C ENSP00000392041.3:n.33+33G>C
ENST00000534956.2:n.36+33G>C
ENST00000536813.6:c.-102+33G>C ENSP00000438726.2:n.-102+33G>C
ENST00000546302.6:c.33+33G>C ENSP00000445599.1:n.33+33G>C
ENST00000640813.1:c.-19+33G>C ENSP00000491061.1:n.-19+33G>C
ENST00000648026.1:c.27+33G>C ENSP00000498044.1:n.27+33G>C
ENST00000649868.1:c.33+33G>C ENSP00000497548.1:n.33+33G>C
ENST00000652429.1:c.33+33G>C MANE Select ENSP00000498786.1:n.33+33G>C
ENST00000278715.7:c.33+33G>C ENSP00000278715.3:n.33+33G>C
ENST00000442944.6:c.-102+33G>C ENSP00000392041.2:n.-102+33G>C
ENST00000535793.5:c.33+33G>C ENSP00000439904.1:n.33+33G>C
ENST00000536185.5:n.201+33G>C
ENST00000536813.5:c.33+33G>C ENSP00000438726.1:n.33+33G>C
ENST00000537841.5:c.-77G>C ENSP00000444730.1:n.-77G>C
ENST00000542044.5:n.158+33G>C
ENST00000542729.5:c.-77G>C ENSP00000443058.1:n.-77G>C
ENST00000542822.5:c.66G>C ENSP00000444817.1:p.Trp22Cys
ENST00000543090.5:c.33+33G>C ENSP00000445429.1:n.33+33G>C
ENST00000543821.5:n.179+33G>C
ENST00000544387.5:c.33+33G>C ENSP00000438424.1:n.33+33G>C
ENST00000545621.5:c.33+33G>C ENSP00000444849.1:n.33+33G>C
ENST00000545901.5:n.186+33G>C
ENST00000546302.5:c.33+33G>C ENSP00000445599.1:n.33+33G>C
NM_000190.3:c.33+33G>C NP_000181.2:n.33+33G>C
NM_001258208.1:c.33+33G>C NP_001245137.1:n.33+33G>C
NM_001258209.1:c.-77G>C NP_001245138.1:n.-77G>C
XM_005271531.1:c.-77G>C XP_005271588.1:n.-77G>C
XM_005271532.1:c.-53G>C XP_005271589.1:n.-53G>C
XM_005271533.2:c.33+33G>C XP_005271590.1:n.33+33G>C
NM_000190.4:c.33+33G>C MANE Select NP_000181.2:n.33+33G>C
XM_005271533.3:c.33+33G>C XP_005271590.1:n.33+33G>C
XM_024448460.1:c.33+33G>C XP_024304228.1:n.33+33G>C
NM_001258208.2:c.33+33G>C NP_001245137.1:n.33+33G>C
NM_001258209.2:c.-77G>C NP_001245138.1:n.-77G>C