Canonical Allele Identifier: CA229596374

Gene: HMBS

Linked Data

• dbSNP Id: rs765208153
• gnomAD v4: 11-119092494-A-G
• MyVariant Identifiers: chr11:g.118963204A>G (hg19) ; chr11:g.119092494A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092494A>G , CM000673.2:g.119092494A>G	GRCh38
NC_000011.9:g.118963204A>G , CM000673.1:g.118963204A>G	GRCh37
NC_000011.8:g.118468414A>G	NCBI36
NG_008093.1:g.12618A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.577A>G	ENSP00000509288.1:p.Ile193Val
ENST00000691144.1:n.2723A>G
ENST00000691249.1:n.1566A>G
ENST00000442944.7:c.724A>G	ENSP00000392041.3:p.Ile242Val
ENST00000640813.1:c.552A>G	ENSP00000491061.1:p.Ala184=
ENST00000648026.1:c.636A>G	ENSP00000498044.1:p.Ala212=
ENST00000648374.1:c.691A>G	ENSP00000497255.1:p.Ile231Val
ENST00000649823.1:n.1199A>G
ENST00000650101.1:c.673A>G	ENSP00000496970.1:p.Ile225Val
ENST00000650307.1:n.1568A>G
ENST00000652429.1:c.742A>G MANE Select	ENSP00000498786.1:p.Ile248Val
ENST00000278715.7:c.742A>G	ENSP00000278715.3:p.Ile248Val
ENST00000392841.1:c.691A>G	ENSP00000376584.1:p.Ile231Val
ENST00000442944.6:c.691A>G	ENSP00000392041.2:p.Ile231Val
ENST00000537841.5:c.691A>G	ENSP00000444730.1:p.Ile231Val
ENST00000542044.5:n.1187A>G
ENST00000542729.5:c.601-264A>G	ENSP00000443058.1:n.601-264A>G
ENST00000543090.5:c.649A>G	ENSP00000445429.1:p.Ile217Val
ENST00000543543.5:n.1217A>G
ENST00000544182.1:n.957A>G
ENST00000544387.5:c.652-264A>G	ENSP00000438424.1:n.652-264A>G
ENST00000545621.5:c.*877A>G	ENSP00000444849.1:n.*877A>G
ENST00000546226.5:n.1270A>G
NM_000190.3:c.742A>G	NP_000181.2:p.Ile248Val
NM_001024382.1:c.691A>G	NP_001019553.1:p.Ile231Val
NM_001258208.1:c.652-264A>G	NP_001245137.1:n.652-264A>G
NM_001258209.1:c.601-264A>G	NP_001245138.1:n.601-264A>G
XM_005271531.1:c.691A>G	XP_005271588.1:p.Ile231Val
XM_005271532.1:c.691A>G	XP_005271589.1:p.Ile231Val
XM_005271533.2:c.688A>G	XP_005271590.1:p.Ile230Val
XM_011542796.1:c.577A>G	XP_011541098.1:p.Ile193Val
NM_000190.4:c.742A>G MANE Select	NP_000181.2:p.Ile248Val
NM_001024382.2:c.691A>G	NP_001019553.1:p.Ile231Val
XM_005271533.3:c.688A>G	XP_005271590.1:p.Ile230Val
XM_017017629.1:c.691A>G	XP_016873118.1:p.Ile231Val
XM_024448460.1:c.598-264A>G	XP_024304228.1:n.598-264A>G
NM_001258208.2:c.652-264A>G	NP_001245137.1:n.652-264A>G
NM_001258209.2:c.601-264A>G	NP_001245138.1:n.601-264A>G