Canonical Allele Identifier: CA2664924303
Gene: GLB1 HGNC NCBI

Linked Data

gnomAD v4: 3-33021693-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33021693C>T , CM000665.2:g.33021693C>T GRCh38
NC_000003.11:g.33063185C>T , CM000665.1:g.33063185C>T GRCh37
NC_000003.10:g.33038189C>T NCBI36
NG_009005.1:g.80510G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307363.10:c.1144-38G>A MANE Select ENSP00000306920.4:n.1144-38G>A
ENST00000307363.9:c.1144-38G>A ENSP00000306920.4:n.1144-38G>A
ENST00000307377.12:c.751-38G>A ENSP00000305920.8:n.751-38G>A
ENST00000399402.7:c.1054-38G>A ENSP00000382333.2:n.1054-38G>A
ENST00000461475.5:n.243-38G>A
ENST00000467571.5:n.181-38G>A
ENST00000473477.1:n.176-38G>A
ENST00000482097.5:n.519-38G>A
ENST00000497796.5:n.396-38G>A
NM_000404.2:c.1144-38G>A NP_000395.2:n.1144-38G>A
NM_000404.3:c.1144-38G>A NP_000395.2:n.1144-38G>A
NM_001079811.1:c.1054-38G>A NP_001073279.1:n.1054-38G>A
NM_001079811.2:c.1054-38G>A NP_001073279.1:n.1054-38G>A
NM_001135602.1:c.751-38G>A NP_001129074.1:n.751-38G>A
NM_001135602.2:c.751-38G>A NP_001129074.1:n.751-38G>A
NM_001317040.1:c.1288-38G>A NP_001303969.1:n.1288-38G>A
XR_001740634.1:n.1543-495C>T
NM_000404.4:c.1144-38G>A MANE Select NP_000395.3:n.1144-38G>A
NM_001079811.3:c.1054-38G>A NP_001073279.2:n.1054-38G>A
NM_001135602.3:c.751-38G>A NP_001129074.2:n.751-38G>A
NM_001317040.2:c.1288-38G>A NP_001303969.2:n.1288-38G>A
NM_001393580.1:c.1144-38G>A NP_001380509.1:n.1144-38G>A