Canonical Allele Identifier: CA382897725
Gene: HMBS HGNC NCBI

Linked Data

dbSNP Id: rs761810461

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119092476G>C , CM000673.2:g.119092476G>C GRCh38
NC_000011.9:g.118963186G>C , CM000673.1:g.118963186G>C GRCh37
NC_000011.8:g.118468396G>C NCBI36
NG_008093.1:g.12600G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000686218.1:c.559G>C ENSP00000509288.1:p.Glu187Gln
ENST00000691144.1:n.2705G>C
ENST00000691249.1:n.1548G>C
ENST00000442944.7:c.706G>C ENSP00000392041.3:p.Glu236Gln
ENST00000536813.6:c.673G>C ENSP00000438726.2:p.Glu225Gln
ENST00000640813.1:c.534G>C ENSP00000491061.1:p.Pro178=
ENST00000648026.1:c.618G>C ENSP00000498044.1:p.Pro206=
ENST00000648374.1:c.673G>C ENSP00000497255.1:p.Glu225Gln
ENST00000649823.1:n.1181G>C
ENST00000650101.1:c.655G>C ENSP00000496970.1:p.Glu219Gln
ENST00000650307.1:n.1550G>C
ENST00000652429.1:c.724G>C MANE Select ENSP00000498786.1:p.Glu242Gln
ENST00000278715.7:c.724G>C ENSP00000278715.3:p.Glu242Gln
ENST00000392841.1:c.673G>C ENSP00000376584.1:p.Glu225Gln
ENST00000442944.6:c.673G>C ENSP00000392041.2:p.Glu225Gln
ENST00000537841.5:c.673G>C ENSP00000444730.1:p.Glu225Gln
ENST00000542044.5:n.1169G>C
ENST00000542729.5:c.601-282G>C ENSP00000443058.1:n.601-282G>C
ENST00000543090.5:c.631G>C ENSP00000445429.1:p.Glu211Gln
ENST00000543543.5:n.1199G>C
ENST00000544182.1:n.939G>C
ENST00000544387.5:c.652-282G>C ENSP00000438424.1:n.652-282G>C
ENST00000545621.5:c.*859G>C ENSP00000444849.1:n.*859G>C
ENST00000546226.5:n.1252G>C
NM_000190.3:c.724G>C NP_000181.2:p.Glu242Gln
NM_001024382.1:c.673G>C NP_001019553.1:p.Glu225Gln
NM_001258208.1:c.652-282G>C NP_001245137.1:n.652-282G>C
NM_001258209.1:c.601-282G>C NP_001245138.1:n.601-282G>C
XM_005271531.1:c.673G>C XP_005271588.1:p.Glu225Gln
XM_005271532.1:c.673G>C XP_005271589.1:p.Glu225Gln
XM_005271533.2:c.670G>C XP_005271590.1:p.Glu224Gln
XM_011542796.1:c.559G>C XP_011541098.1:p.Glu187Gln
NM_000190.4:c.724G>C MANE Select NP_000181.2:p.Glu242Gln
NM_001024382.2:c.673G>C NP_001019553.1:p.Glu225Gln
XM_005271533.3:c.670G>C XP_005271590.1:p.Glu224Gln
XM_017017629.1:c.673G>C XP_016873118.1:p.Glu225Gln
XM_024448460.1:c.598-282G>C XP_024304228.1:n.598-282G>C
NM_001258208.2:c.652-282G>C NP_001245137.1:n.652-282G>C
NM_001258209.2:c.601-282G>C NP_001245138.1:n.601-282G>C