Canonical Allele Identifier: CA477126960

Gene: HMBS

Linked Data

• dbSNP Id: rs1461510221
• gnomAD v2: 11-118963128-G-A
• gnomAD v4: 11-119092418-G-A
• MyVariant Identifiers: chr11:g.118963128G>A (hg19) ; chr11:g.119092418G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092418G>A , CM000673.2:g.119092418G>A	GRCh38
NC_000011.9:g.118963128G>A , CM000673.1:g.118963128G>A	GRCh37
NC_000011.8:g.118468338G>A	NCBI36
NG_008093.1:g.12542G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000686218.1:c.501G>A	ENSP00000509288.1:p.Val167=
ENST00000691144.1:n.2647G>A
ENST00000691249.1:n.1490G>A
ENST00000442944.7:c.648G>A	ENSP00000392041.3:p.Val216=
ENST00000536813.6:c.615G>A	ENSP00000438726.2:p.Val205=
ENST00000640813.1:c.476G>A	ENSP00000491061.1:p.Trp159Ter
ENST00000648026.1:c.560G>A	ENSP00000498044.1:p.Trp187Ter
ENST00000648374.1:c.615G>A	ENSP00000497255.1:p.Val205=
ENST00000649823.1:n.1123G>A
ENST00000650101.1:c.597G>A	ENSP00000496970.1:p.Val199=
ENST00000650307.1:n.1492G>A
ENST00000652429.1:c.666G>A MANE Select	ENSP00000498786.1:p.Val222=
ENST00000278715.7:c.666G>A	ENSP00000278715.3:p.Val222=
ENST00000392841.1:c.615G>A	ENSP00000376584.1:p.Val205=
ENST00000442944.6:c.615G>A	ENSP00000392041.2:p.Val205=
ENST00000537841.5:c.615G>A	ENSP00000444730.1:p.Val205=
ENST00000542044.5:n.1111G>A
ENST00000542729.5:c.600+255G>A	ENSP00000443058.1:n.600+255G>A
ENST00000543090.5:c.573G>A	ENSP00000445429.1:p.Val191=
ENST00000543543.5:n.1141G>A
ENST00000544182.1:n.881G>A
ENST00000544387.5:c.651+255G>A	ENSP00000438424.1:n.651+255G>A
ENST00000545621.5:c.*801G>A	ENSP00000444849.1:n.*801G>A
ENST00000546226.5:n.1194G>A
NM_000190.3:c.666G>A	NP_000181.2:p.Val222=
NM_001024382.1:c.615G>A	NP_001019553.1:p.Val205=
NM_001258208.1:c.651+255G>A	NP_001245137.1:n.651+255G>A
NM_001258209.1:c.600+255G>A	NP_001245138.1:n.600+255G>A
XM_005271531.1:c.615G>A	XP_005271588.1:p.Val205=
XM_005271532.1:c.615G>A	XP_005271589.1:p.Val205=
XM_005271533.2:c.612G>A	XP_005271590.1:p.Val204=
XM_011542796.1:c.501G>A	XP_011541098.1:p.Val167=
NM_000190.4:c.666G>A MANE Select	NP_000181.2:p.Val222=
NM_001024382.2:c.615G>A	NP_001019553.1:p.Val205=
XM_005271533.3:c.612G>A	XP_005271590.1:p.Val204=
XM_017017629.1:c.615G>A	XP_016873118.1:p.Val205=
XM_024448460.1:c.597+255G>A	XP_024304228.1:n.597+255G>A
NM_001258208.2:c.651+255G>A	NP_001245137.1:n.651+255G>A
NM_001258209.2:c.600+255G>A	NP_001245138.1:n.600+255G>A