Canonical Allele Identifier: CA114642
Gene: GLB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 931
ClinVar RCV Id: RCV000000979
dbSNP Id: rs72555362
gnomAD v2: 3-33093471-C-A
gnomAD v3: 3-33051979-C-A
gnomAD v4: 3-33051979-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33051979C>A , CM000665.2:g.33051979C>A GRCh38
NC_000003.11:g.33093471C>A , CM000665.1:g.33093471C>A GRCh37
NC_000003.10:g.33068475C>A NCBI36
NG_009005.1:g.50224G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000307363.10:c.818G>T MANE Select ENSP00000306920.4:p.Trp273Leu
ENST00000307363.9:c.818G>T ENSP00000306920.4:p.Trp273Leu
ENST00000307377.12:c.425G>T ENSP00000305920.8:p.Trp142Leu
ENST00000399402.7:c.728G>T ENSP00000382333.2:p.Trp243Leu
ENST00000415454.1:c.341G>T ENSP00000411813.1:p.Trp114Leu
ENST00000438227.1:c.*310G>T ENSP00000401250.1:n.*310G>T
ENST00000446732.5:c.*261G>T ENSP00000407365.1:n.*261G>T
ENST00000482097.5:n.193G>T
ENST00000485698.5:n.221G>T
ENST00000498537.5:n.344G>T
NM_000404.2:c.818G>T NP_000395.2:p.Trp273Leu
NM_000404.3:c.818G>T NP_000395.2:p.Trp273Leu
NM_001079811.1:c.728G>T NP_001073279.1:p.Trp243Leu
NM_001079811.2:c.728G>T NP_001073279.1:p.Trp243Leu
NM_001135602.1:c.425G>T NP_001129074.1:p.Trp142Leu
NM_001135602.2:c.425G>T NP_001129074.1:p.Trp142Leu
NM_001317040.1:c.962G>T NP_001303969.1:p.Trp321Leu
NM_000404.4:c.818G>T MANE Select NP_000395.3:p.Trp273Leu
NM_001079811.3:c.728G>T NP_001073279.2:p.Trp243Leu
NM_001135602.3:c.425G>T NP_001129074.2:p.Trp142Leu
NM_001317040.2:c.962G>T NP_001303969.2:p.Trp321Leu
NM_001393580.1:c.818G>T NP_001380509.1:p.Trp273Leu