Canonical Allele Identifier: CA432952649

Gene: GLB1

Linked Data

• MyVariant Identifiers: chr3:g.33055650G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33014158G>C , CM000665.2:g.33014158G>C	GRCh38
NC_000003.11:g.33055650G>C , CM000665.1:g.33055650G>C	GRCh37
NC_000003.10:g.33030654G>C	NCBI36
NG_009005.1:g.88045C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.1632C>G MANE Select	ENSP00000306920.4:p.Ser544=
ENST00000307363.9:c.1632C>G	ENSP00000306920.4:p.Ser544=
ENST00000307377.12:c.1239C>G	ENSP00000305920.8:p.Ser413=
ENST00000399402.7:c.1542C>G	ENSP00000382333.2:p.Ser514=
ENST00000461475.5:n.731C>G
ENST00000497796.5:n.884C>G
NM_000404.2:c.1632C>G	NP_000395.2:p.Ser544=
NM_000404.3:c.1632C>G	NP_000395.2:p.Ser544=
NM_001079811.1:c.1542C>G	NP_001073279.1:p.Ser514=
NM_001079811.2:c.1542C>G	NP_001073279.1:p.Ser514=
NM_001135602.1:c.1239C>G	NP_001129074.1:p.Ser413=
NM_001135602.2:c.1239C>G	NP_001129074.1:p.Ser413=
NM_001317040.1:c.1776C>G	NP_001303969.1:p.Ser592=
NM_000404.4:c.1632C>G MANE Select	NP_000395.3:p.Ser544=
NM_001079811.3:c.1542C>G	NP_001073279.2:p.Ser514=
NM_001135602.3:c.1239C>G	NP_001129074.2:p.Ser413=
NM_001317040.2:c.1776C>G	NP_001303969.2:p.Ser592=
NM_001393580.1:c.1632C>G	NP_001380509.1:p.Ser544=