Canonical Allele Identifier: CA352000003

Gene: GLB1

Linked Data

• gnomAD v4: 3-32997100-C-G
• MyVariant Identifiers: chr3:g.33038592C>G (hg19) ; chr3:g.32997100C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.32997100C>G , CM000665.2:g.32997100C>G	GRCh38
NC_000003.11:g.33038592C>G , CM000665.1:g.33038592C>G	GRCh37
NC_000003.10:g.33013596C>G	NCBI36
NG_009005.1:g.105103G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.1979G>C MANE Select	ENSP00000306920.4:p.Arg660Thr
ENST00000307363.9:c.1979G>C	ENSP00000306920.4:p.Arg660Thr
ENST00000307377.12:c.1586G>C	ENSP00000305920.8:p.Arg529Thr
ENST00000399402.7:c.1889G>C	ENSP00000382333.2:p.Arg630Thr
NM_000404.2:c.1979G>C	NP_000395.2:p.Arg660Thr
NM_000404.3:c.1979G>C	NP_000395.2:p.Arg660Thr
NM_001079811.1:c.1889G>C	NP_001073279.1:p.Arg630Thr
NM_001079811.2:c.1889G>C	NP_001073279.1:p.Arg630Thr
NM_001135602.1:c.1586G>C	NP_001129074.1:p.Arg529Thr
NM_001135602.2:c.1586G>C	NP_001129074.1:p.Arg529Thr
NM_001317040.1:c.2123G>C	NP_001303969.1:p.Arg708Thr
NM_000404.4:c.1979G>C MANE Select	NP_000395.3:p.Arg660Thr
NM_001079811.3:c.1889G>C	NP_001073279.2:p.Arg630Thr
NM_001135602.3:c.1586G>C	NP_001129074.2:p.Arg529Thr
NM_001317040.2:c.2123G>C	NP_001303969.2:p.Arg708Thr
NM_001393580.1:c.1734+16956G>C	NP_001380509.1:n.1734+16956G>C