Canonical Allele Identifier: CA6314155

Gene: HMBS

Linked Data

• dbSNP Id: rs151289916
• ExAC: 11:118963140 C / T
• gnomAD v4: 11-119092430-C-T
• MyVariant Identifiers: chr11:g.118963140C>T (hg19) ; chr11:g.119092430C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092430C>T , CM000673.2:g.119092430C>T	GRCh38
NC_000011.9:g.118963140C>T , CM000673.1:g.118963140C>T	GRCh37
NC_000011.8:g.118468350C>T	NCBI36
NG_008093.1:g.12554C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.513C>T	ENSP00000509288.1:p.Ala171=
ENST00000691144.1:n.2659C>T
ENST00000691249.1:n.1502C>T
ENST00000442944.7:c.660C>T	ENSP00000392041.3:p.Ala220=
ENST00000536813.6:c.627C>T	ENSP00000438726.2:p.Ala209=
ENST00000640813.1:c.488C>T	ENSP00000491061.1:p.Pro163Leu
ENST00000648026.1:c.572C>T	ENSP00000498044.1:p.Pro191Leu
ENST00000648374.1:c.627C>T	ENSP00000497255.1:p.Ala209=
ENST00000649823.1:n.1135C>T
ENST00000650101.1:c.609C>T	ENSP00000496970.1:p.Ala203=
ENST00000650307.1:n.1504C>T
ENST00000652429.1:c.678C>T MANE Select	ENSP00000498786.1:p.Ala226=
ENST00000278715.7:c.678C>T	ENSP00000278715.3:p.Ala226=
ENST00000392841.1:c.627C>T	ENSP00000376584.1:p.Ala209=
ENST00000442944.6:c.627C>T	ENSP00000392041.2:p.Ala209=
ENST00000537841.5:c.627C>T	ENSP00000444730.1:p.Ala209=
ENST00000542044.5:n.1123C>T
ENST00000542729.5:c.600+267C>T	ENSP00000443058.1:n.600+267C>T
ENST00000543090.5:c.585C>T	ENSP00000445429.1:p.Ala195=
ENST00000543543.5:n.1153C>T
ENST00000544182.1:n.893C>T
ENST00000544387.5:c.651+267C>T	ENSP00000438424.1:n.651+267C>T
ENST00000545621.5:c.*813C>T	ENSP00000444849.1:n.*813C>T
ENST00000546226.5:n.1206C>T
NM_000190.3:c.678C>T	NP_000181.2:p.Ala226=
NM_001024382.1:c.627C>T	NP_001019553.1:p.Ala209=
NM_001258208.1:c.651+267C>T	NP_001245137.1:n.651+267C>T
NM_001258209.1:c.600+267C>T	NP_001245138.1:n.600+267C>T
XM_005271531.1:c.627C>T	XP_005271588.1:p.Ala209=
XM_005271532.1:c.627C>T	XP_005271589.1:p.Ala209=
XM_005271533.2:c.624C>T	XP_005271590.1:p.Ala208=
XM_011542796.1:c.513C>T	XP_011541098.1:p.Ala171=
NM_000190.4:c.678C>T MANE Select	NP_000181.2:p.Ala226=
NM_001024382.2:c.627C>T	NP_001019553.1:p.Ala209=
XM_005271533.3:c.624C>T	XP_005271590.1:p.Ala208=
XM_017017629.1:c.627C>T	XP_016873118.1:p.Ala209=
XM_024448460.1:c.597+267C>T	XP_024304228.1:n.597+267C>T
NM_001258208.2:c.651+267C>T	NP_001245137.1:n.651+267C>T
NM_001258209.2:c.600+267C>T	NP_001245138.1:n.600+267C>T