Canonical Allele Identifier: CA382899013

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.118963733T>G (hg19) ; chr11:g.119093023T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119093023T>G , CM000673.2:g.119093023T>G	GRCh38
NC_000011.9:g.118963733T>G , CM000673.1:g.118963733T>G	GRCh37
NC_000011.8:g.118468943T>G	NCBI36
NG_008093.1:g.13147T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.747+2T>G	ENSP00000509288.1:n.747+2T>G
ENST00000691144.1:n.3127+2T>G
ENST00000691249.1:n.1736+2T>G
ENST00000442944.7:c.894+2T>G	ENSP00000392041.3:n.894+2T>G
ENST00000640813.1:c.*149+2T>G	ENSP00000491061.1:n.*149+2T>G
ENST00000648026.1:c.806+2T>G	ENSP00000498044.1:n.806+2T>G
ENST00000648374.1:c.861+2T>G	ENSP00000497255.1:n.861+2T>G
ENST00000650101.1:c.843+2T>G	ENSP00000496970.1:n.843+2T>G
ENST00000650307.1:n.1738+2T>G
ENST00000652429.1:c.912+2T>G MANE Select	ENSP00000498786.1:n.912+2T>G
ENST00000278715.7:c.912+2T>G	ENSP00000278715.3:n.912+2T>G
ENST00000392841.1:c.861+2T>G	ENSP00000376584.1:n.861+2T>G
ENST00000442944.6:c.861+2T>G	ENSP00000392041.2:n.861+2T>G
ENST00000537841.5:c.861+2T>G	ENSP00000444730.1:n.861+2T>G
ENST00000539045.1:n.411+2T>G
ENST00000542044.5:n.1357+2T>G
ENST00000542729.5:c.741+2T>G	ENSP00000443058.1:n.741+2T>G
ENST00000543090.5:c.819+2T>G	ENSP00000445429.1:n.819+2T>G
ENST00000543543.5:n.1387+2T>G
ENST00000544182.1:n.1361+2T>G
ENST00000544387.5:c.792+2T>G	ENSP00000438424.1:n.792+2T>G
ENST00000546226.5:n.1674+2T>G
NM_000190.3:c.912+2T>G	NP_000181.2:n.912+2T>G
NM_001024382.1:c.861+2T>G	NP_001019553.1:n.861+2T>G
NM_001258208.1:c.792+2T>G	NP_001245137.1:n.792+2T>G
NM_001258209.1:c.741+2T>G	NP_001245138.1:n.741+2T>G
XM_005271531.1:c.861+2T>G	XP_005271588.1:n.861+2T>G
XM_005271532.1:c.861+2T>G	XP_005271589.1:n.861+2T>G
XM_005271533.2:c.858+2T>G	XP_005271590.1:n.858+2T>G
XM_011542796.1:c.747+2T>G	XP_011541098.1:n.747+2T>G
NM_000190.4:c.912+2T>G MANE Select	NP_000181.2:n.912+2T>G
NM_001024382.2:c.861+2T>G	NP_001019553.1:n.861+2T>G
XM_005271533.3:c.858+2T>G	XP_005271590.1:n.858+2T>G
XM_017017629.1:c.861+2T>G	XP_016873118.1:n.861+2T>G
XM_024448460.1:c.738+2T>G	XP_024304228.1:n.738+2T>G
NM_001258208.2:c.792+2T>G	NP_001245137.1:n.792+2T>G
NM_001258209.2:c.741+2T>G	NP_001245138.1:n.741+2T>G