Canonical Allele Identifier: CA432960132

Gene: GLB1

Linked Data

• ClinVar Variation Id: 1604484
• ClinVar RCV Id: RCV002134657
• dbSNP Id: rs1300459240
• MyVariant Identifiers: chr3:g.33038576G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.32997084G>C , CM000665.2:g.32997084G>C	GRCh38
NC_000003.11:g.33038576G>C , CM000665.1:g.33038576G>C	GRCh37
NC_000003.10:g.33013580G>C	NCBI36
NG_009005.1:g.105119C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.1995C>G MANE Select	ENSP00000306920.4:p.Pro665=
ENST00000307363.9:c.1995C>G	ENSP00000306920.4:p.Pro665=
ENST00000307377.12:c.1602C>G	ENSP00000305920.8:p.Pro534=
ENST00000399402.7:c.1905C>G	ENSP00000382333.2:p.Pro635=
NM_000404.2:c.1995C>G	NP_000395.2:p.Pro665=
NM_000404.3:c.1995C>G	NP_000395.2:p.Pro665=
NM_001079811.1:c.1905C>G	NP_001073279.1:p.Pro635=
NM_001079811.2:c.1905C>G	NP_001073279.1:p.Pro635=
NM_001135602.1:c.1602C>G	NP_001129074.1:p.Pro534=
NM_001135602.2:c.1602C>G	NP_001129074.1:p.Pro534=
NM_001317040.1:c.2139C>G	NP_001303969.1:p.Pro713=
NM_000404.4:c.1995C>G MANE Select	NP_000395.3:p.Pro665=
NM_001079811.3:c.1905C>G	NP_001073279.2:p.Pro635=
NM_001135602.3:c.1602C>G	NP_001129074.2:p.Pro534=
NM_001317040.2:c.2139C>G	NP_001303969.2:p.Pro713=
NM_001393580.1:c.1734+16972C>G	NP_001380509.1:n.1734+16972C>G