Canonical Allele Identifier: CA432952505

Gene: GLB1

Linked Data

• MyVariant Identifiers: chr3:g.33110347T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33068855T>G , CM000665.2:g.33068855T>G	GRCh38
NC_000003.11:g.33110347T>G , CM000665.1:g.33110347T>G	GRCh37
NC_000003.10:g.33085351T>G	NCBI36
NG_009005.1:g.33348A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.361A>C MANE Select	ENSP00000306920.4:p.Arg121=
ENST00000307363.9:c.361A>C	ENSP00000306920.4:p.Arg121=
ENST00000307377.12:c.246-3298A>C	ENSP00000305920.8:n.246-3298A>C
ENST00000399402.7:c.271A>C	ENSP00000382333.2:p.Arg91=
ENST00000415454.1:c.76-10586A>C	ENSP00000411813.1:n.76-10586A>C
ENST00000438227.1:c.76-3298A>C	ENSP00000401250.1:n.76-3298A>C
ENST00000440656.1:c.-33A>C	ENSP00000411769.1:n.-33A>C
ENST00000446732.5:c.156-3298A>C	ENSP00000407365.1:n.156-3298A>C
ENST00000450835.1:c.271A>C	ENSP00000403264.1:p.Arg91=
ENST00000464355.1:n.319A>C
ENST00000482097.5:n.109-15306A>C
ENST00000485698.5:n.137-15306A>C
ENST00000498537.5:n.133-15306A>C
NM_000404.2:c.361A>C	NP_000395.2:p.Arg121=
NM_000404.3:c.361A>C	NP_000395.2:p.Arg121=
NM_001079811.1:c.271A>C	NP_001073279.1:p.Arg91=
NM_001079811.2:c.271A>C	NP_001073279.1:p.Arg91=
NM_001135602.1:c.246-3298A>C	NP_001129074.1:n.246-3298A>C
NM_001135602.2:c.246-3298A>C	NP_001129074.1:n.246-3298A>C
NM_001317040.1:c.505A>C	NP_001303969.1:p.Arg169=
NM_000404.4:c.361A>C MANE Select	NP_000395.3:p.Arg121=
NM_001079811.3:c.271A>C	NP_001073279.2:p.Arg91=
NM_001135602.3:c.246-3298A>C	NP_001129074.2:n.246-3298A>C
NM_001317040.2:c.505A>C	NP_001303969.2:p.Arg169=
NM_001393580.1:c.361A>C	NP_001380509.1:p.Arg121=