Canonical Allele Identifier: CA432952531
Gene: GLB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.33110362G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33068870G>A , CM000665.2:g.33068870G>A GRCh38
NC_000003.11:g.33110362G>A , CM000665.1:g.33110362G>A GRCh37
NC_000003.10:g.33085366G>A NCBI36
NG_009005.1:g.33333C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307363.10:c.346C>T MANE Select ENSP00000306920.4:p.Leu116=
ENST00000307363.9:c.346C>T ENSP00000306920.4:p.Leu116=
ENST00000307377.12:c.246-3313C>T ENSP00000305920.8:n.246-3313C>T
ENST00000399402.7:c.256C>T ENSP00000382333.2:p.Leu86=
ENST00000415454.1:c.76-10601C>T ENSP00000411813.1:n.76-10601C>T
ENST00000438227.1:c.76-3313C>T ENSP00000401250.1:n.76-3313C>T
ENST00000440656.1:c.-48C>T ENSP00000411769.1:n.-48C>T
ENST00000446732.5:c.156-3313C>T ENSP00000407365.1:n.156-3313C>T
ENST00000450835.1:c.256C>T ENSP00000403264.1:p.Leu86=
ENST00000464355.1:n.304C>T
ENST00000482097.5:n.109-15321C>T
ENST00000485698.5:n.137-15321C>T
ENST00000498537.5:n.133-15321C>T
NM_000404.2:c.346C>T NP_000395.2:p.Leu116=
NM_000404.3:c.346C>T NP_000395.2:p.Leu116=
NM_001079811.1:c.256C>T NP_001073279.1:p.Leu86=
NM_001079811.2:c.256C>T NP_001073279.1:p.Leu86=
NM_001135602.1:c.246-3313C>T NP_001129074.1:n.246-3313C>T
NM_001135602.2:c.246-3313C>T NP_001129074.1:n.246-3313C>T
NM_001317040.1:c.490C>T NP_001303969.1:p.Leu164=
NM_000404.4:c.346C>T MANE Select NP_000395.3:p.Leu116=
NM_001079811.3:c.256C>T NP_001073279.2:p.Leu86=
NM_001135602.3:c.246-3313C>T NP_001129074.2:n.246-3313C>T
NM_001317040.2:c.490C>T NP_001303969.2:p.Leu164=
NM_001393580.1:c.346C>T NP_001380509.1:p.Leu116=