Canonical Allele Identifier: CA382899060
Gene: HMBS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119093110C>A , CM000673.2:g.119093110C>A GRCh38
NC_000011.9:g.118963820C>A , CM000673.1:g.118963820C>A GRCh37
NC_000011.8:g.118469030C>A NCBI36
NG_008093.1:g.13234C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000686218.1:c.748C>A ENSP00000509288.1:p.His250Asn
ENST00000691144.1:n.3128C>A
ENST00000691249.1:n.1737C>A
ENST00000442944.7:c.895C>A ENSP00000392041.3:p.His299Asn
ENST00000640813.1:c.*150C>A ENSP00000491061.1:n.*150C>A
ENST00000648026.1:c.807C>A ENSP00000498044.1:n.807C>A
ENST00000648374.1:c.862C>A ENSP00000497255.1:p.His288Asn
ENST00000650101.1:c.844C>A ENSP00000496970.1:p.His282Asn
ENST00000650307.1:n.1739C>A
ENST00000652429.1:c.913C>A MANE Select ENSP00000498786.1:p.His305Asn
ENST00000278715.7:c.913C>A ENSP00000278715.3:p.His305Asn
ENST00000392841.1:c.862C>A ENSP00000376584.1:p.His288Asn
ENST00000442944.6:c.862C>A ENSP00000392041.2:p.His288Asn
ENST00000537841.5:c.862C>A ENSP00000444730.1:p.His288Asn
ENST00000539045.1:n.412C>A
ENST00000542044.5:n.1358C>A
ENST00000542729.5:c.742C>A ENSP00000443058.1:p.His248Asn
ENST00000543090.5:c.820C>A ENSP00000445429.1:p.His274Asn
ENST00000543543.5:n.1388C>A
ENST00000544182.1:n.1362C>A
ENST00000544387.5:c.793C>A ENSP00000438424.1:p.His265Asn
ENST00000546226.5:n.1675C>A
NM_000190.3:c.913C>A NP_000181.2:p.His305Asn
NM_001024382.1:c.862C>A NP_001019553.1:p.His288Asn
NM_001258208.1:c.793C>A NP_001245137.1:p.His265Asn
NM_001258209.1:c.742C>A NP_001245138.1:p.His248Asn
XM_005271531.1:c.862C>A XP_005271588.1:p.His288Asn
XM_005271532.1:c.862C>A XP_005271589.1:p.His288Asn
XM_005271533.2:c.859C>A XP_005271590.1:p.His287Asn
XM_011542796.1:c.748C>A XP_011541098.1:p.His250Asn
NM_000190.4:c.913C>A MANE Select NP_000181.2:p.His305Asn
NM_001024382.2:c.862C>A NP_001019553.1:p.His288Asn
XM_005271533.3:c.859C>A XP_005271590.1:p.His287Asn
XM_017017629.1:c.862C>A XP_016873118.1:p.His288Asn
XM_024448460.1:c.739C>A XP_024304228.1:p.His247Asn
NM_001258208.2:c.793C>A NP_001245137.1:p.His265Asn
NM_001258209.2:c.742C>A NP_001245138.1:p.His248Asn