Canonical Allele Identifier: CA2299268
Gene: GLB1 HGNC NCBI

Linked Data

dbSNP Id: rs774771223
gnomAD v2: 3-33038620-C-G
gnomAD v4: 3-32997128-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.32997128C>G , CM000665.2:g.32997128C>G GRCh38
NC_000003.11:g.33038620C>G , CM000665.1:g.33038620C>G GRCh37
NC_000003.10:g.33013624C>G NCBI36
NG_009005.1:g.105075G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307363.10:c.1951G>C MANE Select ENSP00000306920.4:p.Asp651His
ENST00000307363.9:c.1951G>C ENSP00000306920.4:p.Asp651His
ENST00000307377.12:c.1558G>C ENSP00000305920.8:p.Asp520His
ENST00000399402.7:c.1861G>C ENSP00000382333.2:p.Asp621His
NM_000404.2:c.1951G>C NP_000395.2:p.Asp651His
NM_000404.3:c.1951G>C NP_000395.2:p.Asp651His
NM_001079811.1:c.1861G>C NP_001073279.1:p.Asp621His
NM_001079811.2:c.1861G>C NP_001073279.1:p.Asp621His
NM_001135602.1:c.1558G>C NP_001129074.1:p.Asp520His
NM_001135602.2:c.1558G>C NP_001129074.1:p.Asp520His
NM_001317040.1:c.2095G>C NP_001303969.1:p.Asp699His
NM_000404.4:c.1951G>C MANE Select NP_000395.3:p.Asp651His
NM_001079811.3:c.1861G>C NP_001073279.2:p.Asp621His
NM_001135602.3:c.1558G>C NP_001129074.2:p.Asp520His
NM_001317040.2:c.2095G>C NP_001303969.2:p.Asp699His
NM_001393580.1:c.1734+16928G>C NP_001380509.1:n.1734+16928G>C