Canonical Allele Identifier: CA351995443

Gene: GLB1

Linked Data

• ClinVar Variation Id: 1716905
• ClinVar RCV Id: RCV002296121
• dbSNP Id: rs1699795068
• MyVariant Identifiers: chr3:g.33110446A>G (hg19) ; chr3:g.33068954A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33068954A>G , CM000665.2:g.33068954A>G	GRCh38
NC_000003.11:g.33110446A>G , CM000665.1:g.33110446A>G	GRCh37
NC_000003.10:g.33085450A>G	NCBI36
NG_009005.1:g.33249T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.262T>C MANE Select	ENSP00000306920.4:p.Phe88Leu
ENST00000307363.9:c.262T>C	ENSP00000306920.4:p.Phe88Leu
ENST00000307377.12:c.246-3397T>C	ENSP00000305920.8:n.246-3397T>C
ENST00000399402.7:c.172T>C	ENSP00000382333.2:p.Phe58Leu
ENST00000415454.1:c.76-10685T>C	ENSP00000411813.1:n.76-10685T>C
ENST00000436768.1:c.406T>C	ENSP00000387989.1:p.Phe136Leu
ENST00000438227.1:c.76-3397T>C	ENSP00000401250.1:n.76-3397T>C
ENST00000440656.1:c.-132T>C	ENSP00000411769.1:n.-132T>C
ENST00000446732.5:c.156-3397T>C	ENSP00000407365.1:n.156-3397T>C
ENST00000450835.1:c.172T>C	ENSP00000403264.1:p.Phe58Leu
ENST00000464355.1:n.220T>C
ENST00000482097.5:n.109-15405T>C
ENST00000485698.5:n.137-15405T>C
ENST00000498537.5:n.133-15405T>C
NM_000404.2:c.262T>C	NP_000395.2:p.Phe88Leu
NM_000404.3:c.262T>C	NP_000395.2:p.Phe88Leu
NM_001079811.1:c.172T>C	NP_001073279.1:p.Phe58Leu
NM_001079811.2:c.172T>C	NP_001073279.1:p.Phe58Leu
NM_001135602.1:c.246-3397T>C	NP_001129074.1:n.246-3397T>C
NM_001135602.2:c.246-3397T>C	NP_001129074.1:n.246-3397T>C
NM_001317040.1:c.406T>C	NP_001303969.1:p.Phe136Leu
NM_000404.4:c.262T>C MANE Select	NP_000395.3:p.Phe88Leu
NM_001079811.3:c.172T>C	NP_001073279.2:p.Phe58Leu
NM_001135602.3:c.246-3397T>C	NP_001129074.2:n.246-3397T>C
NM_001317040.2:c.406T>C	NP_001303969.2:p.Phe136Leu
NM_001393580.1:c.262T>C	NP_001380509.1:p.Phe88Leu