Canonical Allele Identifier: CA382896582

Gene: HMBS

Linked Data

• ClinVar Variation Id: 931455
• ClinVar RCV Id: RCV001198011
• dbSNP Id: rs771206317
• MyVariant Identifiers: chr11:g.118962834G>A (hg19) ; chr11:g.119092124G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092124G>A , CM000673.2:g.119092124G>A	GRCh38
NC_000011.9:g.118962834G>A , CM000673.1:g.118962834G>A	GRCh37
NC_000011.8:g.118468044G>A	NCBI36
NG_008093.1:g.12248G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.448-1G>A	ENSP00000509288.1:n.448-1G>A
ENST00000691144.1:n.2354-1G>A
ENST00000691249.1:n.1197-1G>A
ENST00000442944.7:c.595-1G>A	ENSP00000392041.3:n.595-1G>A
ENST00000536813.6:c.562-1G>A	ENSP00000438726.2:n.562-1G>A
ENST00000546302.6:c.535-1G>A	ENSP00000445599.1:n.535-1G>A
ENST00000640813.1:c.461+250G>A	ENSP00000491061.1:n.461+250G>A
ENST00000648026.1:c.507-1G>A	ENSP00000498044.1:n.507-1G>A
ENST00000648374.1:c.562-1G>A	ENSP00000497255.1:n.562-1G>A
ENST00000648488.1:c.*86-1G>A	ENSP00000498079.1:n.*86-1G>A
ENST00000649823.1:n.830-1G>A
ENST00000650101.1:c.544-1G>A	ENSP00000496970.1:n.544-1G>A
ENST00000650307.1:n.1439-1G>A
ENST00000652429.1:c.613-1G>A MANE Select	ENSP00000498786.1:n.613-1G>A
ENST00000278715.7:c.613-1G>A	ENSP00000278715.3:n.613-1G>A
ENST00000392841.1:c.562-1G>A	ENSP00000376584.1:n.562-1G>A
ENST00000442944.6:c.562-1G>A	ENSP00000392041.2:n.562-1G>A
ENST00000537841.5:c.562-1G>A	ENSP00000444730.1:n.562-1G>A
ENST00000542044.5:n.1058-1G>A
ENST00000542345.5:n.751-1G>A
ENST00000542729.5:c.562-1G>A	ENSP00000443058.1:n.562-1G>A
ENST00000543090.5:c.559-280G>A	ENSP00000445429.1:n.559-280G>A
ENST00000543543.5:n.848-1G>A
ENST00000544182.1:n.587G>A
ENST00000544387.5:c.613-1G>A	ENSP00000438424.1:n.613-1G>A
ENST00000545621.5:c.*508-1G>A	ENSP00000444849.1:n.*508-1G>A
ENST00000546226.5:n.901-1G>A
ENST00000546302.5:c.535-1G>A	ENSP00000445599.1:n.535-1G>A
NM_000190.3:c.613-1G>A	NP_000181.2:n.613-1G>A
NM_001024382.1:c.562-1G>A	NP_001019553.1:n.562-1G>A
NM_001258208.1:c.613-1G>A	NP_001245137.1:n.613-1G>A
NM_001258209.1:c.562-1G>A	NP_001245138.1:n.562-1G>A
XM_005271531.1:c.562-1G>A	XP_005271588.1:n.562-1G>A
XM_005271532.1:c.562-1G>A	XP_005271589.1:n.562-1G>A
XM_005271533.2:c.559-1G>A	XP_005271590.1:n.559-1G>A
XM_011542796.1:c.448-1G>A	XP_011541098.1:n.448-1G>A
NM_000190.4:c.613-1G>A MANE Select	NP_000181.2:n.613-1G>A
NM_001024382.2:c.562-1G>A	NP_001019553.1:n.562-1G>A
XM_005271533.3:c.559-1G>A	XP_005271590.1:n.559-1G>A
XM_017017629.1:c.562-1G>A	XP_016873118.1:n.562-1G>A
XM_024448460.1:c.559-1G>A	XP_024304228.1:n.559-1G>A
NM_001258208.2:c.613-1G>A	NP_001245137.1:n.613-1G>A
NM_001258209.2:c.562-1G>A	NP_001245138.1:n.562-1G>A