Canonical Allele Identifier: CA351992853

Gene: GLB1

Linked Data

• gnomAD v4: 3-33021574-C-T
• MyVariant Identifiers: chr3:g.33063066C>T (hg19) ; chr3:g.33021574C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33021574C>T , CM000665.2:g.33021574C>T	GRCh38
NC_000003.11:g.33063066C>T , CM000665.1:g.33063066C>T	GRCh37
NC_000003.10:g.33038070C>T	NCBI36
NG_009005.1:g.80629G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.1225G>A MANE Select	ENSP00000306920.4:p.Val409Met
ENST00000307363.9:c.1225G>A	ENSP00000306920.4:p.Val409Met
ENST00000307377.12:c.832G>A	ENSP00000305920.8:p.Val278Met
ENST00000399402.7:c.1135G>A	ENSP00000382333.2:p.Val379Met
ENST00000461475.5:n.324G>A
ENST00000467571.5:n.262G>A
ENST00000473477.1:n.257G>A
ENST00000497796.5:n.477G>A
NM_000404.2:c.1225G>A	NP_000395.2:p.Val409Met
NM_000404.3:c.1225G>A	NP_000395.2:p.Val409Met
NM_001079811.1:c.1135G>A	NP_001073279.1:p.Val379Met
NM_001079811.2:c.1135G>A	NP_001073279.1:p.Val379Met
NM_001135602.1:c.832G>A	NP_001129074.1:p.Val278Met
NM_001135602.2:c.832G>A	NP_001129074.1:p.Val278Met
NM_001317040.1:c.1369G>A	NP_001303969.1:p.Val457Met
XR_001740634.1:n.1543-614C>T
NM_000404.4:c.1225G>A MANE Select	NP_000395.3:p.Val409Met
NM_001079811.3:c.1135G>A	NP_001073279.2:p.Val379Met
NM_001135602.3:c.832G>A	NP_001129074.2:p.Val278Met
NM_001317040.2:c.1369G>A	NP_001303969.2:p.Val457Met
NM_001393580.1:c.1225G>A	NP_001380509.1:p.Val409Met