Canonical Allele Identifier: CA352000113

Gene: GLB1

Linked Data

• MyVariant Identifiers: chr3:g.33038617G>A (hg19) ; chr3:g.32997125G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.32997125G>A , CM000665.2:g.32997125G>A	GRCh38
NC_000003.11:g.33038617G>A , CM000665.1:g.33038617G>A	GRCh37
NC_000003.10:g.33013621G>A	NCBI36
NG_009005.1:g.105078C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.1954C>T MANE Select	ENSP00000306920.4:p.His652Tyr
ENST00000307363.9:c.1954C>T	ENSP00000306920.4:p.His652Tyr
ENST00000307377.12:c.1561C>T	ENSP00000305920.8:p.His521Tyr
ENST00000399402.7:c.1864C>T	ENSP00000382333.2:p.His622Tyr
NM_000404.2:c.1954C>T	NP_000395.2:p.His652Tyr
NM_000404.3:c.1954C>T	NP_000395.2:p.His652Tyr
NM_001079811.1:c.1864C>T	NP_001073279.1:p.His622Tyr
NM_001079811.2:c.1864C>T	NP_001073279.1:p.His622Tyr
NM_001135602.1:c.1561C>T	NP_001129074.1:p.His521Tyr
NM_001135602.2:c.1561C>T	NP_001129074.1:p.His521Tyr
NM_001317040.1:c.2098C>T	NP_001303969.1:p.His700Tyr
NM_000404.4:c.1954C>T MANE Select	NP_000395.3:p.His652Tyr
NM_001079811.3:c.1864C>T	NP_001073279.2:p.His622Tyr
NM_001135602.3:c.1561C>T	NP_001129074.2:p.His521Tyr
NM_001317040.2:c.2098C>T	NP_001303969.2:p.His700Tyr
NM_001393580.1:c.1734+16931C>T	NP_001380509.1:n.1734+16931C>T