Canonical Allele Identifier: CA432952561
Gene: GLB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.33110384A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33068892A>C , CM000665.2:g.33068892A>C GRCh38
NC_000003.11:g.33110384A>C , CM000665.1:g.33110384A>C GRCh37
NC_000003.10:g.33085388A>C NCBI36
NG_009005.1:g.33311T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307363.10:c.324T>G MANE Select ENSP00000306920.4:p.Leu108=
ENST00000307363.9:c.324T>G ENSP00000306920.4:p.Leu108=
ENST00000307377.12:c.246-3335T>G ENSP00000305920.8:n.246-3335T>G
ENST00000399402.7:c.234T>G ENSP00000382333.2:p.Leu78=
ENST00000415454.1:c.76-10623T>G ENSP00000411813.1:n.76-10623T>G
ENST00000438227.1:c.76-3335T>G ENSP00000401250.1:n.76-3335T>G
ENST00000440656.1:c.-70T>G ENSP00000411769.1:n.-70T>G
ENST00000446732.5:c.156-3335T>G ENSP00000407365.1:n.156-3335T>G
ENST00000450835.1:c.234T>G ENSP00000403264.1:p.Leu78=
ENST00000464355.1:n.282T>G
ENST00000482097.5:n.109-15343T>G
ENST00000485698.5:n.137-15343T>G
ENST00000498537.5:n.133-15343T>G
NM_000404.2:c.324T>G NP_000395.2:p.Leu108=
NM_000404.3:c.324T>G NP_000395.2:p.Leu108=
NM_001079811.1:c.234T>G NP_001073279.1:p.Leu78=
NM_001079811.2:c.234T>G NP_001073279.1:p.Leu78=
NM_001135602.1:c.246-3335T>G NP_001129074.1:n.246-3335T>G
NM_001135602.2:c.246-3335T>G NP_001129074.1:n.246-3335T>G
NM_001317040.1:c.468T>G NP_001303969.1:p.Leu156=
NM_000404.4:c.324T>G MANE Select NP_000395.3:p.Leu108=
NM_001079811.3:c.234T>G NP_001073279.2:p.Leu78=
NM_001135602.3:c.246-3335T>G NP_001129074.2:n.246-3335T>G
NM_001317040.2:c.468T>G NP_001303969.2:p.Leu156=
NM_001393580.1:c.324T>G NP_001380509.1:p.Leu108=