Canonical Allele Identifier: CA351992993
Gene: GLB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33021597A>T , CM000665.2:g.33021597A>T GRCh38
NC_000003.11:g.33063089A>T , CM000665.1:g.33063089A>T GRCh37
NC_000003.10:g.33038093A>T NCBI36
NG_009005.1:g.80606T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307363.10:c.1202T>A MANE Select ENSP00000306920.4:p.Leu401His
ENST00000307363.9:c.1202T>A ENSP00000306920.4:p.Leu401His
ENST00000307377.12:c.809T>A ENSP00000305920.8:p.Leu270His
ENST00000399402.7:c.1112T>A ENSP00000382333.2:p.Leu371His
ENST00000461475.5:n.301T>A
ENST00000467571.5:n.239T>A
ENST00000473477.1:n.234T>A
ENST00000497796.5:n.454T>A
NM_000404.2:c.1202T>A NP_000395.2:p.Leu401His
NM_000404.3:c.1202T>A NP_000395.2:p.Leu401His
NM_001079811.1:c.1112T>A NP_001073279.1:p.Leu371His
NM_001079811.2:c.1112T>A NP_001073279.1:p.Leu371His
NM_001135602.1:c.809T>A NP_001129074.1:p.Leu270His
NM_001135602.2:c.809T>A NP_001129074.1:p.Leu270His
NM_001317040.1:c.1346T>A NP_001303969.1:p.Leu449His
XR_001740634.1:n.1543-591A>T
NM_000404.4:c.1202T>A MANE Select NP_000395.3:p.Leu401His
NM_001079811.3:c.1112T>A NP_001073279.2:p.Leu371His
NM_001135602.3:c.809T>A NP_001129074.2:p.Leu270His
NM_001317040.2:c.1346T>A NP_001303969.2:p.Leu449His
NM_001393580.1:c.1202T>A NP_001380509.1:p.Leu401His