Canonical Allele Identifier: CA352000488

Gene: GLB1

Linked Data

• MyVariant Identifiers: chr3:g.33038703C>T (hg19) ; chr3:g.32997211C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.32997211C>T , CM000665.2:g.32997211C>T	GRCh38
NC_000003.11:g.33038703C>T , CM000665.1:g.33038703C>T	GRCh37
NC_000003.10:g.33013707C>T	NCBI36
NG_009005.1:g.104992G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.1868G>A MANE Select	ENSP00000306920.4:p.Trp623Ter
ENST00000307363.9:c.1868G>A	ENSP00000306920.4:p.Trp623Ter
ENST00000307377.12:c.1475G>A	ENSP00000305920.8:p.Trp492Ter
ENST00000399402.7:c.1778G>A	ENSP00000382333.2:p.Trp593Ter
NM_000404.2:c.1868G>A	NP_000395.2:p.Trp623Ter
NM_000404.3:c.1868G>A	NP_000395.2:p.Trp623Ter
NM_001079811.1:c.1778G>A	NP_001073279.1:p.Trp593Ter
NM_001079811.2:c.1778G>A	NP_001073279.1:p.Trp593Ter
NM_001135602.1:c.1475G>A	NP_001129074.1:p.Trp492Ter
NM_001135602.2:c.1475G>A	NP_001129074.1:p.Trp492Ter
NM_001317040.1:c.2012G>A	NP_001303969.1:p.Trp671Ter
NM_000404.4:c.1868G>A MANE Select	NP_000395.3:p.Trp623Ter
NM_001079811.3:c.1778G>A	NP_001073279.2:p.Trp593Ter
NM_001135602.3:c.1475G>A	NP_001129074.2:p.Trp492Ter
NM_001317040.2:c.2012G>A	NP_001303969.2:p.Trp671Ter
NM_001393580.1:c.1734+16845G>A	NP_001380509.1:n.1734+16845G>A