Canonical Allele Identifier: CA432960124

Gene: GLB1

Linked Data

• MyVariant Identifiers: chr3:g.33038558A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.32997066A>G , CM000665.2:g.32997066A>G	GRCh38
NC_000003.11:g.33038558A>G , CM000665.1:g.33038558A>G	GRCh37
NC_000003.10:g.33013562A>G	NCBI36
NG_009005.1:g.105137T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.2013T>C MANE Select	ENSP00000306920.4:p.Asp671=
ENST00000307363.9:c.2013T>C	ENSP00000306920.4:p.Asp671=
ENST00000307377.12:c.1620T>C	ENSP00000305920.8:p.Asp540=
ENST00000399402.7:c.1923T>C	ENSP00000382333.2:p.Asp641=
NM_000404.2:c.2013T>C	NP_000395.2:p.Asp671=
NM_000404.3:c.2013T>C	NP_000395.2:p.Asp671=
NM_001079811.1:c.1923T>C	NP_001073279.1:p.Asp641=
NM_001079811.2:c.1923T>C	NP_001073279.1:p.Asp641=
NM_001135602.1:c.1620T>C	NP_001129074.1:p.Asp540=
NM_001135602.2:c.1620T>C	NP_001129074.1:p.Asp540=
NM_001317040.1:c.2157T>C	NP_001303969.1:p.Asp719=
NM_000404.4:c.2013T>C MANE Select	NP_000395.3:p.Asp671=
NM_001079811.3:c.1923T>C	NP_001073279.2:p.Asp641=
NM_001135602.3:c.1620T>C	NP_001129074.2:p.Asp540=
NM_001317040.2:c.2157T>C	NP_001303969.2:p.Asp719=
NM_001393580.1:c.1734+16990T>C	NP_001380509.1:n.1734+16990T>C