Canonical Allele Identifier: CA2299312
Gene: GLB1 HGNC NCBI

Linked Data

dbSNP Id: rs376947340
gnomAD v2: 3-33038873-T-A
gnomAD v4: 3-32997381-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.32997381T>A , CM000665.2:g.32997381T>A GRCh38
NC_000003.11:g.33038873T>A , CM000665.1:g.33038873T>A GRCh37
NC_000003.10:g.33013877T>A NCBI36
NG_009005.1:g.104822A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307363.10:c.1735-37A>T MANE Select ENSP00000306920.4:n.1735-37A>T
ENST00000307363.9:c.1735-37A>T ENSP00000306920.4:n.1735-37A>T
ENST00000307377.12:c.1342-37A>T ENSP00000305920.8:n.1342-37A>T
ENST00000399402.7:c.1645-37A>T ENSP00000382333.2:n.1645-37A>T
NM_000404.2:c.1735-37A>T NP_000395.2:n.1735-37A>T
NM_000404.3:c.1735-37A>T NP_000395.2:n.1735-37A>T
NM_001079811.1:c.1645-37A>T NP_001073279.1:n.1645-37A>T
NM_001079811.2:c.1645-37A>T NP_001073279.1:n.1645-37A>T
NM_001135602.1:c.1342-37A>T NP_001129074.1:n.1342-37A>T
NM_001135602.2:c.1342-37A>T NP_001129074.1:n.1342-37A>T
NM_001317040.1:c.1879-37A>T NP_001303969.1:n.1879-37A>T
NM_000404.4:c.1735-37A>T MANE Select NP_000395.3:n.1735-37A>T
NM_001079811.3:c.1645-37A>T NP_001073279.2:n.1645-37A>T
NM_001135602.3:c.1342-37A>T NP_001129074.2:n.1342-37A>T
NM_001317040.2:c.1879-37A>T NP_001303969.2:n.1879-37A>T
NM_001393580.1:c.1734+16675A>T NP_001380509.1:n.1734+16675A>T