Canonical Allele Identifier: CA351991866

Gene: GLB1

Linked Data

• MyVariant Identifiers: chr3:g.33059938A>C (hg19) ; chr3:g.33018446A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33018446A>C , CM000665.2:g.33018446A>C	GRCh38
NC_000003.11:g.33059938A>C , CM000665.1:g.33059938A>C	GRCh37
NC_000003.10:g.33034942A>C	NCBI36
NG_009005.1:g.83757T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.1347+2T>G MANE Select	ENSP00000306920.4:n.1347+2T>G
ENST00000307363.9:c.1347+2T>G	ENSP00000306920.4:n.1347+2T>G
ENST00000307377.12:c.954+2T>G	ENSP00000305920.8:n.954+2T>G
ENST00000399402.7:c.1257+2T>G	ENSP00000382333.2:n.1257+2T>G
ENST00000461475.5:n.446+2T>G
ENST00000467571.5:n.384+2T>G
ENST00000497796.5:n.599+2T>G
NM_000404.2:c.1347+2T>G	NP_000395.2:n.1347+2T>G
NM_000404.3:c.1347+2T>G	NP_000395.2:n.1347+2T>G
NM_001079811.1:c.1257+2T>G	NP_001073279.1:n.1257+2T>G
NM_001079811.2:c.1257+2T>G	NP_001073279.1:n.1257+2T>G
NM_001135602.1:c.954+2T>G	NP_001129074.1:n.954+2T>G
NM_001135602.2:c.954+2T>G	NP_001129074.1:n.954+2T>G
NM_001317040.1:c.1491+2T>G	NP_001303969.1:n.1491+2T>G
NM_000404.4:c.1347+2T>G MANE Select	NP_000395.3:n.1347+2T>G
NM_001079811.3:c.1257+2T>G	NP_001073279.2:n.1257+2T>G
NM_001135602.3:c.954+2T>G	NP_001129074.2:n.954+2T>G
NM_001317040.2:c.1491+2T>G	NP_001303969.2:n.1491+2T>G
NM_001393580.1:c.1347+2T>G	NP_001380509.1:n.1347+2T>G