Canonical Allele Identifier: CA477128981
Gene: HMBS HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.118963231C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119092521C>T , CM000673.2:g.119092521C>T GRCh38
NC_000011.9:g.118963231C>T , CM000673.1:g.118963231C>T GRCh37
NC_000011.8:g.118468441C>T NCBI36
NG_008093.1:g.12645C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000686218.1:c.604C>T ENSP00000509288.1:p.Leu202=
ENST00000691144.1:n.2750C>T
ENST00000691249.1:n.1593C>T
ENST00000442944.7:c.751C>T ENSP00000392041.3:p.Leu251=
ENST00000640813.1:c.*6C>T ENSP00000491061.1:n.*6C>T
ENST00000648026.1:c.663C>T ENSP00000498044.1:n.663C>T
ENST00000648374.1:c.718C>T ENSP00000497255.1:p.Leu240=
ENST00000649823.1:n.1226C>T
ENST00000650101.1:c.700C>T ENSP00000496970.1:p.Leu234=
ENST00000650307.1:n.1595C>T
ENST00000652429.1:c.769C>T MANE Select ENSP00000498786.1:p.Leu257=
ENST00000278715.7:c.769C>T ENSP00000278715.3:p.Leu257=
ENST00000392841.1:c.718C>T ENSP00000376584.1:p.Leu240=
ENST00000442944.6:c.718C>T ENSP00000392041.2:p.Leu240=
ENST00000537841.5:c.718C>T ENSP00000444730.1:p.Leu240=
ENST00000542044.5:n.1214C>T
ENST00000542729.5:c.601-237C>T ENSP00000443058.1:n.601-237C>T
ENST00000543090.5:c.676C>T ENSP00000445429.1:p.Leu226=
ENST00000543543.5:n.1244C>T
ENST00000544182.1:n.984C>T
ENST00000544387.5:c.652-237C>T ENSP00000438424.1:n.652-237C>T
ENST00000546226.5:n.1297C>T
NM_000190.3:c.769C>T NP_000181.2:p.Leu257=
NM_001024382.1:c.718C>T NP_001019553.1:p.Leu240=
NM_001258208.1:c.652-237C>T NP_001245137.1:n.652-237C>T
NM_001258209.1:c.601-237C>T NP_001245138.1:n.601-237C>T
XM_005271531.1:c.718C>T XP_005271588.1:p.Leu240=
XM_005271532.1:c.718C>T XP_005271589.1:p.Leu240=
XM_005271533.2:c.715C>T XP_005271590.1:p.Leu239=
XM_011542796.1:c.604C>T XP_011541098.1:p.Leu202=
NM_000190.4:c.769C>T MANE Select NP_000181.2:p.Leu257=
NM_001024382.2:c.718C>T NP_001019553.1:p.Leu240=
XM_005271533.3:c.715C>T XP_005271590.1:p.Leu239=
XM_017017629.1:c.718C>T XP_016873118.1:p.Leu240=
XM_024448460.1:c.598-237C>T XP_024304228.1:n.598-237C>T
NM_001258208.2:c.652-237C>T NP_001245137.1:n.652-237C>T
NM_001258209.2:c.601-237C>T NP_001245138.1:n.601-237C>T