Canonical Allele Identifier: CA2299348

Gene: GLB1

Linked Data

• dbSNP Id: rs749577111
• ExAC: 3:33055676 C / A
• gnomAD v2: 3-33055676-C-A
• MyVariant Identifiers: chr3:g.33055676C>A (hg19) ; chr3:g.33014184C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33014184C>A , CM000665.2:g.33014184C>A	GRCh38
NC_000003.11:g.33055676C>A , CM000665.1:g.33055676C>A	GRCh37
NC_000003.10:g.33030680C>A	NCBI36
NG_009005.1:g.88019G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.1606G>T MANE Select	ENSP00000306920.4:p.Asp536Tyr
ENST00000307363.9:c.1606G>T	ENSP00000306920.4:p.Asp536Tyr
ENST00000307377.12:c.1213G>T	ENSP00000305920.8:p.Asp405Tyr
ENST00000399402.7:c.1516G>T	ENSP00000382333.2:p.Asp506Tyr
ENST00000461475.5:n.705G>T
ENST00000497796.5:n.858G>T
NM_000404.2:c.1606G>T	NP_000395.2:p.Asp536Tyr
NM_000404.3:c.1606G>T	NP_000395.2:p.Asp536Tyr
NM_001079811.1:c.1516G>T	NP_001073279.1:p.Asp506Tyr
NM_001079811.2:c.1516G>T	NP_001073279.1:p.Asp506Tyr
NM_001135602.1:c.1213G>T	NP_001129074.1:p.Asp405Tyr
NM_001135602.2:c.1213G>T	NP_001129074.1:p.Asp405Tyr
NM_001317040.1:c.1750G>T	NP_001303969.1:p.Asp584Tyr
NM_000404.4:c.1606G>T MANE Select	NP_000395.3:p.Asp536Tyr
NM_001079811.3:c.1516G>T	NP_001073279.2:p.Asp506Tyr
NM_001135602.3:c.1213G>T	NP_001129074.2:p.Asp405Tyr
NM_001317040.2:c.1750G>T	NP_001303969.2:p.Asp584Tyr
NM_001393580.1:c.1606G>T	NP_001380509.1:p.Asp536Tyr