Canonical Allele Identifier: CA2616355391
Gene: HMBS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119093074T>C , CM000673.2:g.119093074T>C GRCh38
NC_000011.9:g.118963784T>C , CM000673.1:g.118963784T>C GRCh37
NC_000011.8:g.118468994T>C NCBI36
NG_008093.1:g.13198T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000686218.1:c.748-36T>C ENSP00000509288.1:n.748-36T>C
ENST00000691144.1:n.3128-36T>C
ENST00000691249.1:n.1737-36T>C
ENST00000442944.7:c.895-36T>C ENSP00000392041.3:n.895-36T>C
ENST00000640813.1:c.*150-36T>C ENSP00000491061.1:n.*150-36T>C
ENST00000648026.1:c.807-36T>C ENSP00000498044.1:n.807-36T>C
ENST00000648374.1:c.862-36T>C ENSP00000497255.1:n.862-36T>C
ENST00000650101.1:c.844-36T>C ENSP00000496970.1:n.844-36T>C
ENST00000650307.1:n.1739-36T>C
ENST00000652429.1:c.913-36T>C MANE Select ENSP00000498786.1:n.913-36T>C
ENST00000278715.7:c.913-36T>C ENSP00000278715.3:n.913-36T>C
ENST00000392841.1:c.862-36T>C ENSP00000376584.1:n.862-36T>C
ENST00000442944.6:c.862-36T>C ENSP00000392041.2:n.862-36T>C
ENST00000537841.5:c.862-36T>C ENSP00000444730.1:n.862-36T>C
ENST00000539045.1:n.412-36T>C
ENST00000542044.5:n.1358-36T>C
ENST00000542729.5:c.742-36T>C ENSP00000443058.1:n.742-36T>C
ENST00000543090.5:c.820-36T>C ENSP00000445429.1:n.820-36T>C
ENST00000543543.5:n.1388-36T>C
ENST00000544182.1:n.1362-36T>C
ENST00000544387.5:c.793-36T>C ENSP00000438424.1:n.793-36T>C
ENST00000546226.5:n.1675-36T>C
NM_000190.3:c.913-36T>C NP_000181.2:n.913-36T>C
NM_001024382.1:c.862-36T>C NP_001019553.1:n.862-36T>C
NM_001258208.1:c.793-36T>C NP_001245137.1:n.793-36T>C
NM_001258209.1:c.742-36T>C NP_001245138.1:n.742-36T>C
XM_005271531.1:c.862-36T>C XP_005271588.1:n.862-36T>C
XM_005271532.1:c.862-36T>C XP_005271589.1:n.862-36T>C
XM_005271533.2:c.859-36T>C XP_005271590.1:n.859-36T>C
XM_011542796.1:c.748-36T>C XP_011541098.1:n.748-36T>C
NM_000190.4:c.913-36T>C MANE Select NP_000181.2:n.913-36T>C
NM_001024382.2:c.862-36T>C NP_001019553.1:n.862-36T>C
XM_005271533.3:c.859-36T>C XP_005271590.1:n.859-36T>C
XM_017017629.1:c.862-36T>C XP_016873118.1:n.862-36T>C
XM_024448460.1:c.739-36T>C XP_024304228.1:n.739-36T>C
NM_001258208.2:c.793-36T>C NP_001245137.1:n.793-36T>C
NM_001258209.2:c.742-36T>C NP_001245138.1:n.742-36T>C