Canonical Allele Identifier: CA432953494

Gene: GLB1

Linked Data

• MyVariant Identifiers: chr3:g.33063064C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33021572C>G , CM000665.2:g.33021572C>G	GRCh38
NC_000003.11:g.33063064C>G , CM000665.1:g.33063064C>G	GRCh37
NC_000003.10:g.33038068C>G	NCBI36
NG_009005.1:g.80631G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.1227G>C MANE Select	ENSP00000306920.4:p.Val409=
ENST00000307363.9:c.1227G>C	ENSP00000306920.4:p.Val409=
ENST00000307377.12:c.834G>C	ENSP00000305920.8:p.Val278=
ENST00000399402.7:c.1137G>C	ENSP00000382333.2:p.Val379=
ENST00000461475.5:n.326G>C
ENST00000467571.5:n.264G>C
ENST00000473477.1:n.259G>C
ENST00000497796.5:n.479G>C
NM_000404.2:c.1227G>C	NP_000395.2:p.Val409=
NM_000404.3:c.1227G>C	NP_000395.2:p.Val409=
NM_001079811.1:c.1137G>C	NP_001073279.1:p.Val379=
NM_001079811.2:c.1137G>C	NP_001073279.1:p.Val379=
NM_001135602.1:c.834G>C	NP_001129074.1:p.Val278=
NM_001135602.2:c.834G>C	NP_001129074.1:p.Val278=
NM_001317040.1:c.1371G>C	NP_001303969.1:p.Val457=
XR_001740634.1:n.1543-616C>G
NM_000404.4:c.1227G>C MANE Select	NP_000395.3:p.Val409=
NM_001079811.3:c.1137G>C	NP_001073279.2:p.Val379=
NM_001135602.3:c.834G>C	NP_001129074.2:p.Val278=
NM_001317040.2:c.1371G>C	NP_001303969.2:p.Val457=
NM_001393580.1:c.1227G>C	NP_001380509.1:p.Val409=