Canonical Allele Identifier: CA432960195

Gene: GLB1

Linked Data

• MyVariant Identifiers: chr3:g.33038633T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.32997141T>A , CM000665.2:g.32997141T>A	GRCh38
NC_000003.11:g.33038633T>A , CM000665.1:g.33038633T>A	GRCh37
NC_000003.10:g.33013637T>A	NCBI36
NG_009005.1:g.105062A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.1938A>T MANE Select	ENSP00000306920.4:p.Ser646=
ENST00000307363.9:c.1938A>T	ENSP00000306920.4:p.Ser646=
ENST00000307377.12:c.1545A>T	ENSP00000305920.8:p.Ser515=
ENST00000399402.7:c.1848A>T	ENSP00000382333.2:p.Ser616=
NM_000404.2:c.1938A>T	NP_000395.2:p.Ser646=
NM_000404.3:c.1938A>T	NP_000395.2:p.Ser646=
NM_001079811.1:c.1848A>T	NP_001073279.1:p.Ser616=
NM_001079811.2:c.1848A>T	NP_001073279.1:p.Ser616=
NM_001135602.1:c.1545A>T	NP_001129074.1:p.Ser515=
NM_001135602.2:c.1545A>T	NP_001129074.1:p.Ser515=
NM_001317040.1:c.2082A>T	NP_001303969.1:p.Ser694=
NM_000404.4:c.1938A>T MANE Select	NP_000395.3:p.Ser646=
NM_001079811.3:c.1848A>T	NP_001073279.2:p.Ser616=
NM_001135602.3:c.1545A>T	NP_001129074.2:p.Ser515=
NM_001317040.2:c.2082A>T	NP_001303969.2:p.Ser694=
NM_001393580.1:c.1734+16915A>T	NP_001380509.1:n.1734+16915A>T