Canonical Allele Identifier: CA477151607

Gene: HMBS

Linked Data

• dbSNP Id: rs1946014036
• MyVariant Identifiers: chr11:g.118955764G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119085054G>A , CM000673.2:g.119085054G>A	GRCh38
NC_000011.9:g.118955764G>A , CM000673.1:g.118955764G>A	GRCh37
NC_000011.8:g.118460974G>A	NCBI36
NG_008093.1:g.5178G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442944.7:c.21G>A	ENSP00000392041.3:p.Ala7=
ENST00000534956.2:n.24G>A
ENST00000536813.6:c.-114G>A	ENSP00000438726.2:n.-114G>A
ENST00000546302.6:c.21G>A	ENSP00000445599.1:p.Ala7=
ENST00000640813.1:c.-31G>A	ENSP00000491061.1:n.-31G>A
ENST00000648026.1:c.15G>A	ENSP00000498044.1:p.Ala5=
ENST00000649868.1:c.21G>A	ENSP00000497548.1:p.Ala7=
ENST00000652429.1:c.21G>A MANE Select	ENSP00000498786.1:p.Ala7=
ENST00000278715.7:c.21G>A	ENSP00000278715.3:p.Ala7=
ENST00000442944.6:c.-114G>A	ENSP00000392041.2:n.-114G>A
ENST00000535793.5:c.21G>A	ENSP00000439904.1:p.Ala7=
ENST00000536185.5:n.189G>A
ENST00000536813.5:c.21G>A	ENSP00000438726.1:p.Ala7=
ENST00000537841.5:c.-122G>A	ENSP00000444730.1:n.-122G>A
ENST00000542044.5:n.146G>A
ENST00000542729.5:c.-122G>A	ENSP00000443058.1:n.-122G>A
ENST00000542822.5:c.21G>A	ENSP00000444817.1:p.Ala7=
ENST00000543090.5:c.21G>A	ENSP00000445429.1:p.Ala7=
ENST00000543821.5:n.167G>A
ENST00000544387.5:c.21G>A	ENSP00000438424.1:p.Ala7=
ENST00000545621.5:c.21G>A	ENSP00000444849.1:p.Ala7=
ENST00000545901.5:n.174G>A
ENST00000546302.5:c.21G>A	ENSP00000445599.1:p.Ala7=
NM_000190.3:c.21G>A	NP_000181.2:p.Ala7=
NM_001258208.1:c.21G>A	NP_001245137.1:p.Ala7=
NM_001258209.1:c.-122G>A	NP_001245138.1:n.-122G>A
XM_005271531.1:c.-122G>A	XP_005271588.1:n.-122G>A
XM_005271532.1:c.-98G>A	XP_005271589.1:n.-98G>A
XM_005271533.2:c.21G>A	XP_005271590.1:p.Ala7=
NM_000190.4:c.21G>A MANE Select	NP_000181.2:p.Ala7=
XM_005271533.3:c.21G>A	XP_005271590.1:p.Ala7=
XM_024448460.1:c.21G>A	XP_024304228.1:p.Ala7=
NM_001258208.2:c.21G>A	NP_001245137.1:p.Ala7=
NM_001258209.2:c.-122G>A	NP_001245138.1:n.-122G>A