Canonical Allele Identifier: CA477369207

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.118963692A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092982A>C , CM000673.2:g.119092982A>C	GRCh38
NC_000011.9:g.118963692A>C , CM000673.1:g.118963692A>C	GRCh37
NC_000011.8:g.118468902A>C	NCBI36
NG_008093.1:g.13106A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.708A>C	ENSP00000509288.1:p.Ile236=
ENST00000691144.1:n.3088A>C
ENST00000691249.1:n.1697A>C
ENST00000442944.7:c.855A>C	ENSP00000392041.3:p.Ile285=
ENST00000640813.1:c.*110A>C	ENSP00000491061.1:n.*110A>C
ENST00000648026.1:c.767A>C	ENSP00000498044.1:n.767A>C
ENST00000648374.1:c.822A>C	ENSP00000497255.1:p.Ile274=
ENST00000650101.1:c.804A>C	ENSP00000496970.1:p.Ile268=
ENST00000650307.1:n.1699A>C
ENST00000652429.1:c.873A>C MANE Select	ENSP00000498786.1:p.Ile291=
ENST00000278715.7:c.873A>C	ENSP00000278715.3:p.Ile291=
ENST00000392841.1:c.822A>C	ENSP00000376584.1:p.Ile274=
ENST00000442944.6:c.822A>C	ENSP00000392041.2:p.Ile274=
ENST00000537841.5:c.822A>C	ENSP00000444730.1:p.Ile274=
ENST00000539045.1:n.372A>C
ENST00000542044.5:n.1318A>C
ENST00000542729.5:c.702A>C	ENSP00000443058.1:p.Ile234=
ENST00000543090.5:c.780A>C	ENSP00000445429.1:p.Ile260=
ENST00000543543.5:n.1348A>C
ENST00000544182.1:n.1322A>C
ENST00000544387.5:c.753A>C	ENSP00000438424.1:p.Ile251=
ENST00000546226.5:n.1635A>C
NM_000190.3:c.873A>C	NP_000181.2:p.Ile291=
NM_001024382.1:c.822A>C	NP_001019553.1:p.Ile274=
NM_001258208.1:c.753A>C	NP_001245137.1:p.Ile251=
NM_001258209.1:c.702A>C	NP_001245138.1:p.Ile234=
XM_005271531.1:c.822A>C	XP_005271588.1:p.Ile274=
XM_005271532.1:c.822A>C	XP_005271589.1:p.Ile274=
XM_005271533.2:c.819A>C	XP_005271590.1:p.Ile273=
XM_011542796.1:c.708A>C	XP_011541098.1:p.Ile236=
NM_000190.4:c.873A>C MANE Select	NP_000181.2:p.Ile291=
NM_001024382.2:c.822A>C	NP_001019553.1:p.Ile274=
XM_005271533.3:c.819A>C	XP_005271590.1:p.Ile273=
XM_017017629.1:c.822A>C	XP_016873118.1:p.Ile274=
XM_024448460.1:c.699A>C	XP_024304228.1:p.Ile233=
NM_001258208.2:c.753A>C	NP_001245137.1:p.Ile251=
NM_001258209.2:c.702A>C	NP_001245138.1:p.Ile234=