Canonical Allele Identifier: CA2003790912
Gene: HMBS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119092148G= , CM000673.2:g.119092148G= GRCh38
NC_000011.9:g.118962858G= , CM000673.1:g.118962858G= GRCh37
NC_000011.8:g.118468068G= NCBI36
NG_008093.1:g.12272G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000686218.1:c.471G= ENSP00000509288.1:p.Met157=
ENST00000691144.1:n.2377G=
ENST00000691249.1:n.1220G=
ENST00000442944.7:c.618G= ENSP00000392041.3:p.Met206=
ENST00000536813.6:c.585G= ENSP00000438726.2:p.Met195=
ENST00000546302.6:c.558G= ENSP00000445599.1:p.Met186=
ENST00000640813.1:c.462-256G= ENSP00000491061.1:n.462-256G=
ENST00000648026.1:c.530G= ENSP00000498044.1:p.Cys177=
ENST00000648374.1:c.585G= ENSP00000497255.1:p.Met195=
ENST00000648488.1:c.*109G= ENSP00000498079.1:n.*109G=
ENST00000649823.1:n.853G=
ENST00000650101.1:c.567G= ENSP00000496970.1:p.Met189=
ENST00000650307.1:n.1462G=
ENST00000652429.1:c.636G= MANE Select ENSP00000498786.1:p.Met212=
ENST00000278715.7:c.636G= ENSP00000278715.3:p.Met212=
ENST00000392841.1:c.585G= ENSP00000376584.1:p.Met195=
ENST00000442944.6:c.585G= ENSP00000392041.2:p.Met195=
ENST00000537841.5:c.585G= ENSP00000444730.1:p.Met195=
ENST00000542044.5:n.1081G=
ENST00000542345.5:n.774G=
ENST00000542729.5:c.585G= ENSP00000443058.1:p.Met195=
ENST00000543090.5:c.559-256G= ENSP00000445429.1:n.559-256G=
ENST00000543543.5:n.871G=
ENST00000544182.1:n.611G=
ENST00000544387.5:c.636G= ENSP00000438424.1:p.Met212=
ENST00000545621.5:c.*531G= ENSP00000444849.1:n.*531G=
ENST00000546226.5:n.924G=
ENST00000546302.5:c.558G= ENSP00000445599.1:p.Met186=
NM_000190.3:c.636G= NP_000181.2:p.Met212=
NM_001024382.1:c.585G= NP_001019553.1:p.Met195=
NM_001258208.1:c.636G= NP_001245137.1:p.Met212=
NM_001258209.1:c.585G= NP_001245138.1:p.Met195=
XM_005271531.1:c.585G= XP_005271588.1:p.Met195=
XM_005271532.1:c.585G= XP_005271589.1:p.Met195=
XM_005271533.2:c.582G= XP_005271590.1:p.Met194=
XM_011542796.1:c.471G= XP_011541098.1:p.Met157=
NM_000190.4:c.636G= MANE Select NP_000181.2:p.Met212=
NM_001024382.2:c.585G= NP_001019553.1:p.Met195=
XM_005271533.3:c.582G= XP_005271590.1:p.Met194=
XM_017017629.1:c.585G= XP_016873118.1:p.Met195=
XM_024448460.1:c.582G= XP_024304228.1:p.Met194=
NM_001258208.2:c.636G= NP_001245137.1:p.Met212=
NM_001258209.2:c.585G= NP_001245138.1:p.Met195=