Canonical Allele Identifier: CA432953516

Gene: GLB1

Linked Data

• MyVariant Identifiers: chr3:g.33063070G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33021578G>A , CM000665.2:g.33021578G>A	GRCh38
NC_000003.11:g.33063070G>A , CM000665.1:g.33063070G>A	GRCh37
NC_000003.10:g.33038074G>A	NCBI36
NG_009005.1:g.80625C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.1221C>T MANE Select	ENSP00000306920.4:p.Ile407=
ENST00000307363.9:c.1221C>T	ENSP00000306920.4:p.Ile407=
ENST00000307377.12:c.828C>T	ENSP00000305920.8:p.Ile276=
ENST00000399402.7:c.1131C>T	ENSP00000382333.2:p.Ile377=
ENST00000461475.5:n.320C>T
ENST00000467571.5:n.258C>T
ENST00000473477.1:n.253C>T
ENST00000497796.5:n.473C>T
NM_000404.2:c.1221C>T	NP_000395.2:p.Ile407=
NM_000404.3:c.1221C>T	NP_000395.2:p.Ile407=
NM_001079811.1:c.1131C>T	NP_001073279.1:p.Ile377=
NM_001079811.2:c.1131C>T	NP_001073279.1:p.Ile377=
NM_001135602.1:c.828C>T	NP_001129074.1:p.Ile276=
NM_001135602.2:c.828C>T	NP_001129074.1:p.Ile276=
NM_001317040.1:c.1365C>T	NP_001303969.1:p.Ile455=
XR_001740634.1:n.1543-610G>A
NM_000404.4:c.1221C>T MANE Select	NP_000395.3:p.Ile407=
NM_001079811.3:c.1131C>T	NP_001073279.2:p.Ile377=
NM_001135602.3:c.828C>T	NP_001129074.2:p.Ile276=
NM_001317040.2:c.1365C>T	NP_001303969.2:p.Ile455=
NM_001393580.1:c.1221C>T	NP_001380509.1:p.Ile407=