Canonical Allele Identifier: CA352000803

Gene: GLB1

Linked Data

• MyVariant Identifiers: chr3:g.33038812T>A (hg19) ; chr3:g.32997320T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.32997320T>A , CM000665.2:g.32997320T>A	GRCh38
NC_000003.11:g.33038812T>A , CM000665.1:g.33038812T>A	GRCh37
NC_000003.10:g.33013816T>A	NCBI36
NG_009005.1:g.104883A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000307363.10:c.1759A>T MANE Select	ENSP00000306920.4:p.Asn587Tyr
ENST00000307363.9:c.1759A>T	ENSP00000306920.4:p.Asn587Tyr
ENST00000307377.12:c.1366A>T	ENSP00000305920.8:p.Asn456Tyr
ENST00000399402.7:c.1669A>T	ENSP00000382333.2:p.Asn557Tyr
NM_000404.2:c.1759A>T	NP_000395.2:p.Asn587Tyr
NM_000404.3:c.1759A>T	NP_000395.2:p.Asn587Tyr
NM_001079811.1:c.1669A>T	NP_001073279.1:p.Asn557Tyr
NM_001079811.2:c.1669A>T	NP_001073279.1:p.Asn557Tyr
NM_001135602.1:c.1366A>T	NP_001129074.1:p.Asn456Tyr
NM_001135602.2:c.1366A>T	NP_001129074.1:p.Asn456Tyr
NM_001317040.1:c.1903A>T	NP_001303969.1:p.Asn635Tyr
NM_000404.4:c.1759A>T MANE Select	NP_000395.3:p.Asn587Tyr
NM_001079811.3:c.1669A>T	NP_001073279.2:p.Asn557Tyr
NM_001135602.3:c.1366A>T	NP_001129074.2:p.Asn456Tyr
NM_001317040.2:c.1903A>T	NP_001303969.2:p.Asn635Tyr
NM_001393580.1:c.1734+16736A>T	NP_001380509.1:n.1734+16736A>T