Canonical Allele Identifier: CA2299267
Gene: GLB1 HGNC NCBI

Linked Data

dbSNP Id: rs771296891
gnomAD v2: 3-33038610-G-A
gnomAD v4: 3-32997118-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.32997118G>A , CM000665.2:g.32997118G>A GRCh38
NC_000003.11:g.33038610G>A , CM000665.1:g.33038610G>A GRCh37
NC_000003.10:g.33013614G>A NCBI36
NG_009005.1:g.105085C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307363.10:c.1961C>T MANE Select ENSP00000306920.4:p.Ser654Phe
ENST00000307363.9:c.1961C>T ENSP00000306920.4:p.Ser654Phe
ENST00000307377.12:c.1568C>T ENSP00000305920.8:p.Ser523Phe
ENST00000399402.7:c.1871C>T ENSP00000382333.2:p.Ser624Phe
NM_000404.2:c.1961C>T NP_000395.2:p.Ser654Phe
NM_000404.3:c.1961C>T NP_000395.2:p.Ser654Phe
NM_001079811.1:c.1871C>T NP_001073279.1:p.Ser624Phe
NM_001079811.2:c.1871C>T NP_001073279.1:p.Ser624Phe
NM_001135602.1:c.1568C>T NP_001129074.1:p.Ser523Phe
NM_001135602.2:c.1568C>T NP_001129074.1:p.Ser523Phe
NM_001317040.1:c.2105C>T NP_001303969.1:p.Ser702Phe
NM_000404.4:c.1961C>T MANE Select NP_000395.3:p.Ser654Phe
NM_001079811.3:c.1871C>T NP_001073279.2:p.Ser624Phe
NM_001135602.3:c.1568C>T NP_001129074.2:p.Ser523Phe
NM_001317040.2:c.2105C>T NP_001303969.2:p.Ser702Phe
NM_001393580.1:c.1734+16938C>T NP_001380509.1:n.1734+16938C>T