Canonical Allele Identifier: CA477126577

Gene: HMBS

Linked Data

• gnomAD v4: 11-119092133-C-T
• MyVariant Identifiers: chr11:g.118962843C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092133C>T , CM000673.2:g.119092133C>T	GRCh38
NC_000011.9:g.118962843C>T , CM000673.1:g.118962843C>T	GRCh37
NC_000011.8:g.118468053C>T	NCBI36
NG_008093.1:g.12257C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.456C>T	ENSP00000509288.1:p.His152=
ENST00000691144.1:n.2362C>T
ENST00000691249.1:n.1205C>T
ENST00000442944.7:c.603C>T	ENSP00000392041.3:p.His201=
ENST00000536813.6:c.570C>T	ENSP00000438726.2:p.His190=
ENST00000546302.6:c.543C>T	ENSP00000445599.1:p.His181=
ENST00000640813.1:c.461+259C>T	ENSP00000491061.1:n.461+259C>T
ENST00000648026.1:c.515C>T	ENSP00000498044.1:p.Thr172Ile
ENST00000648374.1:c.570C>T	ENSP00000497255.1:p.His190=
ENST00000648488.1:c.*94C>T	ENSP00000498079.1:n.*94C>T
ENST00000649823.1:n.838C>T
ENST00000650101.1:c.552C>T	ENSP00000496970.1:p.His184=
ENST00000650307.1:n.1447C>T
ENST00000652429.1:c.621C>T MANE Select	ENSP00000498786.1:p.His207=
ENST00000278715.7:c.621C>T	ENSP00000278715.3:p.His207=
ENST00000392841.1:c.570C>T	ENSP00000376584.1:p.His190=
ENST00000442944.6:c.570C>T	ENSP00000392041.2:p.His190=
ENST00000537841.5:c.570C>T	ENSP00000444730.1:p.His190=
ENST00000542044.5:n.1066C>T
ENST00000542345.5:n.759C>T
ENST00000542729.5:c.570C>T	ENSP00000443058.1:p.His190=
ENST00000543090.5:c.559-271C>T	ENSP00000445429.1:n.559-271C>T
ENST00000543543.5:n.856C>T
ENST00000544182.1:n.596C>T
ENST00000544387.5:c.621C>T	ENSP00000438424.1:p.His207=
ENST00000545621.5:c.*516C>T	ENSP00000444849.1:n.*516C>T
ENST00000546226.5:n.909C>T
ENST00000546302.5:c.543C>T	ENSP00000445599.1:p.His181=
NM_000190.3:c.621C>T	NP_000181.2:p.His207=
NM_001024382.1:c.570C>T	NP_001019553.1:p.His190=
NM_001258208.1:c.621C>T	NP_001245137.1:p.His207=
NM_001258209.1:c.570C>T	NP_001245138.1:p.His190=
XM_005271531.1:c.570C>T	XP_005271588.1:p.His190=
XM_005271532.1:c.570C>T	XP_005271589.1:p.His190=
XM_005271533.2:c.567C>T	XP_005271590.1:p.His189=
XM_011542796.1:c.456C>T	XP_011541098.1:p.His152=
NM_000190.4:c.621C>T MANE Select	NP_000181.2:p.His207=
NM_001024382.2:c.570C>T	NP_001019553.1:p.His190=
XM_005271533.3:c.567C>T	XP_005271590.1:p.His189=
XM_017017629.1:c.570C>T	XP_016873118.1:p.His190=
XM_024448460.1:c.567C>T	XP_024304228.1:p.His189=
NM_001258208.2:c.621C>T	NP_001245137.1:p.His207=
NM_001258209.2:c.570C>T	NP_001245138.1:p.His190=