Canonical Allele Identifier: CA477369270

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.118963966T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119093256T>C , CM000673.2:g.119093256T>C	GRCh38
NC_000011.9:g.118963966T>C , CM000673.1:g.118963966T>C	GRCh37
NC_000011.8:g.118469176T>C	NCBI36
NG_008093.1:g.13380T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.894T>C	ENSP00000509288.1:p.Val298=
ENST00000691144.1:n.3274T>C
ENST00000691249.1:n.1883T>C
ENST00000442944.7:c.1041T>C	ENSP00000392041.3:p.Val347=
ENST00000640813.1:c.*296T>C	ENSP00000491061.1:n.*296T>C
ENST00000648026.1:c.953T>C	ENSP00000498044.1:n.953T>C
ENST00000648374.1:c.1008T>C	ENSP00000497255.1:p.Val336=
ENST00000650101.1:c.990T>C	ENSP00000496970.1:p.Val330=
ENST00000650307.1:n.1885T>C
ENST00000652429.1:c.1059T>C MANE Select	ENSP00000498786.1:p.Val353=
ENST00000278715.7:c.1059T>C	ENSP00000278715.3:p.Val353=
ENST00000392841.1:c.1008T>C	ENSP00000376584.1:p.Val336=
ENST00000442944.6:c.1008T>C	ENSP00000392041.2:p.Val336=
ENST00000537841.5:c.1008T>C	ENSP00000444730.1:p.Val336=
ENST00000539045.1:n.558T>C
ENST00000542044.5:n.1504T>C
ENST00000542729.5:c.888T>C	ENSP00000443058.1:p.Val296=
ENST00000543090.5:c.966T>C	ENSP00000445429.1:p.Val322=
ENST00000543543.5:n.1534T>C
ENST00000544182.1:n.1508T>C
ENST00000544387.5:c.939T>C	ENSP00000438424.1:p.Val313=
ENST00000546226.5:n.1821T>C
NM_000190.3:c.1059T>C	NP_000181.2:p.Val353=
NM_001024382.1:c.1008T>C	NP_001019553.1:p.Val336=
NM_001258208.1:c.939T>C	NP_001245137.1:p.Val313=
NM_001258209.1:c.888T>C	NP_001245138.1:p.Val296=
XM_005271531.1:c.1008T>C	XP_005271588.1:p.Val336=
XM_005271532.1:c.1008T>C	XP_005271589.1:p.Val336=
XM_005271533.2:c.1005T>C	XP_005271590.1:p.Val335=
XM_011542796.1:c.894T>C	XP_011541098.1:p.Val298=
NM_000190.4:c.1059T>C MANE Select	NP_000181.2:p.Val353=
NM_001024382.2:c.1008T>C	NP_001019553.1:p.Val336=
XM_005271533.3:c.1005T>C	XP_005271590.1:p.Val335=
XM_017017629.1:c.1008T>C	XP_016873118.1:p.Val336=
XM_024448460.1:c.885T>C	XP_024304228.1:p.Val295=
NM_001258208.2:c.939T>C	NP_001245137.1:p.Val313=
NM_001258209.2:c.888T>C	NP_001245138.1:p.Val296=