Canonical Allele Identifier: CA432952805
Gene: GLB1 HGNC NCBI

Linked Data

gnomAD v4: 3-33072591-C-T
MyVariant Identifiers: chr3:g.33114083C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33072591C>T , CM000665.2:g.33072591C>T GRCh38
NC_000003.11:g.33114083C>T , CM000665.1:g.33114083C>T GRCh37
NC_000003.10:g.33089087C>T NCBI36
NG_009005.1:g.29612G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307363.10:c.198G>A MANE Select ENSP00000306920.4:p.Lys66=
ENST00000307363.9:c.198G>A ENSP00000306920.4:p.Lys66=
ENST00000307377.12:c.198G>A ENSP00000305920.8:p.Lys66=
ENST00000399402.7:c.108G>A ENSP00000382333.2:p.Lys36=
ENST00000415454.1:c.76-14322G>A ENSP00000411813.1:n.76-14322G>A
ENST00000436768.1:c.342G>A ENSP00000387989.1:p.Lys114=
ENST00000438227.1:c.76-7034G>A ENSP00000401250.1:n.76-7034G>A
ENST00000440656.1:c.-148-3621G>A ENSP00000411769.1:n.-148-3621G>A
ENST00000446732.5:c.108G>A ENSP00000407365.1:p.Lys36=
ENST00000450835.1:c.108G>A ENSP00000403264.1:p.Lys36=
ENST00000464355.1:n.156G>A
ENST00000482097.5:n.109-19042G>A
ENST00000485698.5:n.137-19042G>A
ENST00000498537.5:n.133-19042G>A
NM_000404.2:c.198G>A NP_000395.2:p.Lys66=
NM_000404.3:c.198G>A NP_000395.2:p.Lys66=
NM_001079811.1:c.108G>A NP_001073279.1:p.Lys36=
NM_001079811.2:c.108G>A NP_001073279.1:p.Lys36=
NM_001135602.1:c.198G>A NP_001129074.1:p.Lys66=
NM_001135602.2:c.198G>A NP_001129074.1:p.Lys66=
NM_001317040.1:c.342G>A NP_001303969.1:p.Lys114=
NM_000404.4:c.198G>A MANE Select NP_000395.3:p.Lys66=
NM_001079811.3:c.108G>A NP_001073279.2:p.Lys36=
NM_001135602.3:c.198G>A NP_001129074.2:p.Lys66=
NM_001317040.2:c.342G>A NP_001303969.2:p.Lys114=
NM_001393580.1:c.198G>A NP_001380509.1:p.Lys66=