Canonical Allele Identifier: CA432953629

Gene: GLB1

Linked Data

• MyVariant Identifiers: chr3:g.33063100G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33021608G>C , CM000665.2:g.33021608G>C	GRCh38
NC_000003.11:g.33063100G>C , CM000665.1:g.33063100G>C	GRCh37
NC_000003.10:g.33038104G>C	NCBI36
NG_009005.1:g.80595C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.1191C>G MANE Select	ENSP00000306920.4:p.Pro397=
ENST00000307363.9:c.1191C>G	ENSP00000306920.4:p.Pro397=
ENST00000307377.12:c.798C>G	ENSP00000305920.8:p.Pro266=
ENST00000399402.7:c.1101C>G	ENSP00000382333.2:p.Pro367=
ENST00000461475.5:n.290C>G
ENST00000467571.5:n.228C>G
ENST00000473477.1:n.223C>G
ENST00000497796.5:n.443C>G
NM_000404.2:c.1191C>G	NP_000395.2:p.Pro397=
NM_000404.3:c.1191C>G	NP_000395.2:p.Pro397=
NM_001079811.1:c.1101C>G	NP_001073279.1:p.Pro367=
NM_001079811.2:c.1101C>G	NP_001073279.1:p.Pro367=
NM_001135602.1:c.798C>G	NP_001129074.1:p.Pro266=
NM_001135602.2:c.798C>G	NP_001129074.1:p.Pro266=
NM_001317040.1:c.1335C>G	NP_001303969.1:p.Pro445=
XR_001740634.1:n.1543-580G>C
NM_000404.4:c.1191C>G MANE Select	NP_000395.3:p.Pro397=
NM_001079811.3:c.1101C>G	NP_001073279.2:p.Pro367=
NM_001135602.3:c.798C>G	NP_001129074.2:p.Pro266=
NM_001317040.2:c.1335C>G	NP_001303969.2:p.Pro445=
NM_001393580.1:c.1191C>G	NP_001380509.1:p.Pro397=