Canonical Allele Identifier: CA382898791

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.118963679G>T (hg19) ; chr11:g.119092969G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092969G>T , CM000673.2:g.119092969G>T	GRCh38
NC_000011.9:g.118963679G>T , CM000673.1:g.118963679G>T	GRCh37
NC_000011.8:g.118468889G>T	NCBI36
NG_008093.1:g.13093G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.695G>T	ENSP00000509288.1:p.Gly232Val
ENST00000691144.1:n.3075G>T
ENST00000691249.1:n.1684G>T
ENST00000442944.7:c.842G>T	ENSP00000392041.3:p.Gly281Val
ENST00000640813.1:c.*97G>T	ENSP00000491061.1:n.*97G>T
ENST00000648026.1:c.754G>T	ENSP00000498044.1:n.754G>T
ENST00000648374.1:c.809G>T	ENSP00000497255.1:p.Gly270Val
ENST00000650101.1:c.791G>T	ENSP00000496970.1:p.Gly264Val
ENST00000650307.1:n.1686G>T
ENST00000652429.1:c.860G>T MANE Select	ENSP00000498786.1:p.Gly287Val
ENST00000278715.7:c.860G>T	ENSP00000278715.3:p.Gly287Val
ENST00000392841.1:c.809G>T	ENSP00000376584.1:p.Gly270Val
ENST00000442944.6:c.809G>T	ENSP00000392041.2:p.Gly270Val
ENST00000537841.5:c.809G>T	ENSP00000444730.1:p.Gly270Val
ENST00000539045.1:n.359G>T
ENST00000542044.5:n.1305G>T
ENST00000542729.5:c.689G>T	ENSP00000443058.1:p.Gly230Val
ENST00000543090.5:c.767G>T	ENSP00000445429.1:p.Gly256Val
ENST00000543543.5:n.1335G>T
ENST00000544182.1:n.1309G>T
ENST00000544387.5:c.740G>T	ENSP00000438424.1:p.Gly247Val
ENST00000546226.5:n.1622G>T
NM_000190.3:c.860G>T	NP_000181.2:p.Gly287Val
NM_001024382.1:c.809G>T	NP_001019553.1:p.Gly270Val
NM_001258208.1:c.740G>T	NP_001245137.1:p.Gly247Val
NM_001258209.1:c.689G>T	NP_001245138.1:p.Gly230Val
XM_005271531.1:c.809G>T	XP_005271588.1:p.Gly270Val
XM_005271532.1:c.809G>T	XP_005271589.1:p.Gly270Val
XM_005271533.2:c.806G>T	XP_005271590.1:p.Gly269Val
XM_011542796.1:c.695G>T	XP_011541098.1:p.Gly232Val
NM_000190.4:c.860G>T MANE Select	NP_000181.2:p.Gly287Val
NM_001024382.2:c.809G>T	NP_001019553.1:p.Gly270Val
XM_005271533.3:c.806G>T	XP_005271590.1:p.Gly269Val
XM_017017629.1:c.809G>T	XP_016873118.1:p.Gly270Val
XM_024448460.1:c.686G>T	XP_024304228.1:p.Gly229Val
NM_001258208.2:c.740G>T	NP_001245137.1:p.Gly247Val
NM_001258209.2:c.689G>T	NP_001245138.1:p.Gly230Val