Canonical Allele Identifier: CA351995243

Gene: GLB1

Linked Data

• MyVariant Identifiers: chr3:g.33110427C>A (hg19) ; chr3:g.33068935C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33068935C>A , CM000665.2:g.33068935C>A	GRCh38
NC_000003.11:g.33110427C>A , CM000665.1:g.33110427C>A	GRCh37
NC_000003.10:g.33085431C>A	NCBI36
NG_009005.1:g.33268G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.281G>T MANE Select	ENSP00000306920.4:p.Gly94Val
ENST00000307363.9:c.281G>T	ENSP00000306920.4:p.Gly94Val
ENST00000307377.12:c.246-3378G>T	ENSP00000305920.8:n.246-3378G>T
ENST00000399402.7:c.191G>T	ENSP00000382333.2:p.Gly64Val
ENST00000415454.1:c.76-10666G>T	ENSP00000411813.1:n.76-10666G>T
ENST00000436768.1:c.425G>T	ENSP00000387989.1:p.Gly142Val
ENST00000438227.1:c.76-3378G>T	ENSP00000401250.1:n.76-3378G>T
ENST00000440656.1:c.-113G>T	ENSP00000411769.1:n.-113G>T
ENST00000446732.5:c.156-3378G>T	ENSP00000407365.1:n.156-3378G>T
ENST00000450835.1:c.191G>T	ENSP00000403264.1:p.Gly64Val
ENST00000464355.1:n.239G>T
ENST00000482097.5:n.109-15386G>T
ENST00000485698.5:n.137-15386G>T
ENST00000498537.5:n.133-15386G>T
NM_000404.2:c.281G>T	NP_000395.2:p.Gly94Val
NM_000404.3:c.281G>T	NP_000395.2:p.Gly94Val
NM_001079811.1:c.191G>T	NP_001073279.1:p.Gly64Val
NM_001079811.2:c.191G>T	NP_001073279.1:p.Gly64Val
NM_001135602.1:c.246-3378G>T	NP_001129074.1:n.246-3378G>T
NM_001135602.2:c.246-3378G>T	NP_001129074.1:n.246-3378G>T
NM_001317040.1:c.425G>T	NP_001303969.1:p.Gly142Val
NM_000404.4:c.281G>T MANE Select	NP_000395.3:p.Gly94Val
NM_001079811.3:c.191G>T	NP_001073279.2:p.Gly64Val
NM_001135602.3:c.246-3378G>T	NP_001129074.2:n.246-3378G>T
NM_001317040.2:c.425G>T	NP_001303969.2:p.Gly142Val
NM_001393580.1:c.281G>T	NP_001380509.1:p.Gly94Val