Canonical Allele Identifier: CA382899116

Gene: HMBS

Linked Data

• dbSNP Id: rs746707121
• MyVariant Identifiers: chr11:g.118963832C>G (hg19) ; chr11:g.119093122C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119093122C>G , CM000673.2:g.119093122C>G	GRCh38
NC_000011.9:g.118963832C>G , CM000673.1:g.118963832C>G	GRCh37
NC_000011.8:g.118469042C>G	NCBI36
NG_008093.1:g.13246C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.760C>G	ENSP00000509288.1:p.Pro254Ala
ENST00000691144.1:n.3140C>G
ENST00000691249.1:n.1749C>G
ENST00000442944.7:c.907C>G	ENSP00000392041.3:p.Pro303Ala
ENST00000640813.1:c.*162C>G	ENSP00000491061.1:n.*162C>G
ENST00000648026.1:c.819C>G	ENSP00000498044.1:n.819C>G
ENST00000648374.1:c.874C>G	ENSP00000497255.1:p.Pro292Ala
ENST00000650101.1:c.856C>G	ENSP00000496970.1:p.Pro286Ala
ENST00000650307.1:n.1751C>G
ENST00000652429.1:c.925C>G MANE Select	ENSP00000498786.1:p.Pro309Ala
ENST00000278715.7:c.925C>G	ENSP00000278715.3:p.Pro309Ala
ENST00000392841.1:c.874C>G	ENSP00000376584.1:p.Pro292Ala
ENST00000442944.6:c.874C>G	ENSP00000392041.2:p.Pro292Ala
ENST00000537841.5:c.874C>G	ENSP00000444730.1:p.Pro292Ala
ENST00000539045.1:n.424C>G
ENST00000542044.5:n.1370C>G
ENST00000542729.5:c.754C>G	ENSP00000443058.1:p.Pro252Ala
ENST00000543090.5:c.832C>G	ENSP00000445429.1:p.Pro278Ala
ENST00000543543.5:n.1400C>G
ENST00000544182.1:n.1374C>G
ENST00000544387.5:c.805C>G	ENSP00000438424.1:p.Pro269Ala
ENST00000546226.5:n.1687C>G
NM_000190.3:c.925C>G	NP_000181.2:p.Pro309Ala
NM_001024382.1:c.874C>G	NP_001019553.1:p.Pro292Ala
NM_001258208.1:c.805C>G	NP_001245137.1:p.Pro269Ala
NM_001258209.1:c.754C>G	NP_001245138.1:p.Pro252Ala
XM_005271531.1:c.874C>G	XP_005271588.1:p.Pro292Ala
XM_005271532.1:c.874C>G	XP_005271589.1:p.Pro292Ala
XM_005271533.2:c.871C>G	XP_005271590.1:p.Pro291Ala
XM_011542796.1:c.760C>G	XP_011541098.1:p.Pro254Ala
NM_000190.4:c.925C>G MANE Select	NP_000181.2:p.Pro309Ala
NM_001024382.2:c.874C>G	NP_001019553.1:p.Pro292Ala
XM_005271533.3:c.871C>G	XP_005271590.1:p.Pro291Ala
XM_017017629.1:c.874C>G	XP_016873118.1:p.Pro292Ala
XM_024448460.1:c.751C>G	XP_024304228.1:p.Pro251Ala
NM_001258208.2:c.805C>G	NP_001245137.1:p.Pro269Ala
NM_001258209.2:c.754C>G	NP_001245138.1:p.Pro252Ala