Canonical Allele Identifier: CA477127303

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.118963167G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092457G>T , CM000673.2:g.119092457G>T	GRCh38
NC_000011.9:g.118963167G>T , CM000673.1:g.118963167G>T	GRCh37
NC_000011.8:g.118468377G>T	NCBI36
NG_008093.1:g.12581G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.540G>T	ENSP00000509288.1:p.Val180=
ENST00000691144.1:n.2686G>T
ENST00000691249.1:n.1529G>T
ENST00000442944.7:c.687G>T	ENSP00000392041.3:p.Val229=
ENST00000536813.6:c.654G>T	ENSP00000438726.2:p.Val218=
ENST00000640813.1:c.515G>T	ENSP00000491061.1:p.Trp172Leu
ENST00000648026.1:c.599G>T	ENSP00000498044.1:p.Trp200Leu
ENST00000648374.1:c.654G>T	ENSP00000497255.1:p.Val218=
ENST00000649823.1:n.1162G>T
ENST00000650101.1:c.636G>T	ENSP00000496970.1:p.Val212=
ENST00000650307.1:n.1531G>T
ENST00000652429.1:c.705G>T MANE Select	ENSP00000498786.1:p.Val235=
ENST00000278715.7:c.705G>T	ENSP00000278715.3:p.Val235=
ENST00000392841.1:c.654G>T	ENSP00000376584.1:p.Val218=
ENST00000442944.6:c.654G>T	ENSP00000392041.2:p.Val218=
ENST00000537841.5:c.654G>T	ENSP00000444730.1:p.Val218=
ENST00000542044.5:n.1150G>T
ENST00000542729.5:c.600+294G>T	ENSP00000443058.1:n.600+294G>T
ENST00000543090.5:c.612G>T	ENSP00000445429.1:p.Val204=
ENST00000543543.5:n.1180G>T
ENST00000544182.1:n.920G>T
ENST00000544387.5:c.651+294G>T	ENSP00000438424.1:n.651+294G>T
ENST00000545621.5:c.*840G>T	ENSP00000444849.1:n.*840G>T
ENST00000546226.5:n.1233G>T
NM_000190.3:c.705G>T	NP_000181.2:p.Val235=
NM_001024382.1:c.654G>T	NP_001019553.1:p.Val218=
NM_001258208.1:c.651+294G>T	NP_001245137.1:n.651+294G>T
NM_001258209.1:c.600+294G>T	NP_001245138.1:n.600+294G>T
XM_005271531.1:c.654G>T	XP_005271588.1:p.Val218=
XM_005271532.1:c.654G>T	XP_005271589.1:p.Val218=
XM_005271533.2:c.651G>T	XP_005271590.1:p.Val217=
XM_011542796.1:c.540G>T	XP_011541098.1:p.Val180=
NM_000190.4:c.705G>T MANE Select	NP_000181.2:p.Val235=
NM_001024382.2:c.654G>T	NP_001019553.1:p.Val218=
XM_005271533.3:c.651G>T	XP_005271590.1:p.Val217=
XM_017017629.1:c.654G>T	XP_016873118.1:p.Val218=
XM_024448460.1:c.597+294G>T	XP_024304228.1:n.597+294G>T
NM_001258208.2:c.651+294G>T	NP_001245137.1:n.651+294G>T
NM_001258209.2:c.600+294G>T	NP_001245138.1:n.600+294G>T