Canonical Allele Identifier: CA432952779

Gene: GLB1

Linked Data

• MyVariant Identifiers: chr3:g.33114044G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33072552G>T , CM000665.2:g.33072552G>T	GRCh38
NC_000003.11:g.33114044G>T , CM000665.1:g.33114044G>T	GRCh37
NC_000003.10:g.33089048G>T	NCBI36
NG_009005.1:g.29651C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.237C>A MANE Select	ENSP00000306920.4:p.Ala79=
ENST00000307363.9:c.237C>A	ENSP00000306920.4:p.Ala79=
ENST00000307377.12:c.237C>A	ENSP00000305920.8:p.Ala79=
ENST00000399402.7:c.147C>A	ENSP00000382333.2:p.Ala49=
ENST00000415454.1:c.76-14283C>A	ENSP00000411813.1:n.76-14283C>A
ENST00000436768.1:c.381C>A	ENSP00000387989.1:p.Ala127=
ENST00000438227.1:c.76-6995C>A	ENSP00000401250.1:n.76-6995C>A
ENST00000440656.1:c.-148-3582C>A	ENSP00000411769.1:n.-148-3582C>A
ENST00000446732.5:c.147C>A	ENSP00000407365.1:p.Ala49=
ENST00000450835.1:c.147C>A	ENSP00000403264.1:p.Ala49=
ENST00000464355.1:n.195C>A
ENST00000482097.5:n.109-19003C>A
ENST00000485698.5:n.137-19003C>A
ENST00000498537.5:n.133-19003C>A
NM_000404.2:c.237C>A	NP_000395.2:p.Ala79=
NM_000404.3:c.237C>A	NP_000395.2:p.Ala79=
NM_001079811.1:c.147C>A	NP_001073279.1:p.Ala49=
NM_001079811.2:c.147C>A	NP_001073279.1:p.Ala49=
NM_001135602.1:c.237C>A	NP_001129074.1:p.Ala79=
NM_001135602.2:c.237C>A	NP_001129074.1:p.Ala79=
NM_001317040.1:c.381C>A	NP_001303969.1:p.Ala127=
NM_000404.4:c.237C>A MANE Select	NP_000395.3:p.Ala79=
NM_001079811.3:c.147C>A	NP_001073279.2:p.Ala49=
NM_001135602.3:c.237C>A	NP_001129074.2:p.Ala79=
NM_001317040.2:c.381C>A	NP_001303969.2:p.Ala127=
NM_001393580.1:c.237C>A	NP_001380509.1:p.Ala79=