Canonical Allele Identifier: CA432953012

Gene: GLB1

Linked Data

• MyVariant Identifiers: chr3:g.33059988A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33018496A>T , CM000665.2:g.33018496A>T	GRCh38
NC_000003.11:g.33059988A>T , CM000665.1:g.33059988A>T	GRCh37
NC_000003.10:g.33034992A>T	NCBI36
NG_009005.1:g.83707T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.1299T>A MANE Select	ENSP00000306920.4:p.Ser433=
ENST00000307363.9:c.1299T>A	ENSP00000306920.4:p.Ser433=
ENST00000307377.12:c.906T>A	ENSP00000305920.8:p.Ser302=
ENST00000399402.7:c.1209T>A	ENSP00000382333.2:p.Ser403=
ENST00000461475.5:n.398T>A
ENST00000467571.5:n.336T>A
ENST00000497796.5:n.551T>A
NM_000404.2:c.1299T>A	NP_000395.2:p.Ser433=
NM_000404.3:c.1299T>A	NP_000395.2:p.Ser433=
NM_001079811.1:c.1209T>A	NP_001073279.1:p.Ser403=
NM_001079811.2:c.1209T>A	NP_001073279.1:p.Ser403=
NM_001135602.1:c.906T>A	NP_001129074.1:p.Ser302=
NM_001135602.2:c.906T>A	NP_001129074.1:p.Ser302=
NM_001317040.1:c.1443T>A	NP_001303969.1:p.Ser481=
NM_000404.4:c.1299T>A MANE Select	NP_000395.3:p.Ser433=
NM_001079811.3:c.1209T>A	NP_001073279.2:p.Ser403=
NM_001135602.3:c.906T>A	NP_001129074.2:p.Ser302=
NM_001317040.2:c.1443T>A	NP_001303969.2:p.Ser481=
NM_001393580.1:c.1299T>A	NP_001380509.1:p.Ser433=