Canonical Allele Identifier: CA2003792634
Gene: HMBS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119092921G= , CM000673.2:g.119092921G= GRCh38
NC_000011.9:g.118963631G= , CM000673.1:g.118963631G= GRCh37
NC_000011.8:g.118468841G= NCBI36
NG_008093.1:g.13045G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000686218.1:c.661-14G= ENSP00000509288.1:n.661-14G=
ENST00000691144.1:n.3041-14G=
ENST00000691249.1:n.1650-14G=
ENST00000442944.7:c.808-14G= ENSP00000392041.3:n.808-14G=
ENST00000640813.1:c.*63-14G= ENSP00000491061.1:n.*63-14G=
ENST00000648026.1:c.720-14G= ENSP00000498044.1:n.720-14G=
ENST00000648374.1:c.775-14G= ENSP00000497255.1:n.775-14G=
ENST00000649823.1:n.1283-14G=
ENST00000650101.1:c.757-14G= ENSP00000496970.1:n.757-14G=
ENST00000650307.1:n.1652-14G=
ENST00000652429.1:c.826-14G= MANE Select ENSP00000498786.1:n.826-14G=
ENST00000278715.7:c.826-14G= ENSP00000278715.3:n.826-14G=
ENST00000392841.1:c.775-14G= ENSP00000376584.1:n.775-14G=
ENST00000442944.6:c.775-14G= ENSP00000392041.2:n.775-14G=
ENST00000537841.5:c.775-14G= ENSP00000444730.1:n.775-14G=
ENST00000539045.1:n.311G=
ENST00000542044.5:n.1271-14G=
ENST00000542729.5:c.655-14G= ENSP00000443058.1:n.655-14G=
ENST00000543090.5:c.733-14G= ENSP00000445429.1:n.733-14G=
ENST00000543543.5:n.1301-14G=
ENST00000544182.1:n.1275-14G=
ENST00000544387.5:c.706-14G= ENSP00000438424.1:n.706-14G=
ENST00000546226.5:n.1588-14G=
NM_000190.3:c.826-14G= NP_000181.2:n.826-14G=
NM_001024382.1:c.775-14G= NP_001019553.1:n.775-14G=
NM_001258208.1:c.706-14G= NP_001245137.1:n.706-14G=
NM_001258209.1:c.655-14G= NP_001245138.1:n.655-14G=
XM_005271531.1:c.775-14G= XP_005271588.1:n.775-14G=
XM_005271532.1:c.775-14G= XP_005271589.1:n.775-14G=
XM_005271533.2:c.772-14G= XP_005271590.1:n.772-14G=
XM_011542796.1:c.661-14G= XP_011541098.1:n.661-14G=
NM_000190.4:c.826-14G= MANE Select NP_000181.2:n.826-14G=
NM_001024382.2:c.775-14G= NP_001019553.1:n.775-14G=
XM_005271533.3:c.772-14G= XP_005271590.1:n.772-14G=
XM_017017629.1:c.775-14G= XP_016873118.1:n.775-14G=
XM_024448460.1:c.652-14G= XP_024304228.1:n.652-14G=
NM_001258208.2:c.706-14G= NP_001245137.1:n.706-14G=
NM_001258209.2:c.655-14G= NP_001245138.1:n.655-14G=