Canonical Allele Identifier: CA432957648

Linked Data

dbSNP Id: rs780964758
gnomAD v2: 3-33138509-G-A
gnomAD v3: 3-33097017-G-A
gnomAD v4: 3-33097017-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33097017G>A , CM000665.2:g.33097017G>A GRCh38
NC_000003.11:g.33138509G>A , CM000665.1:g.33138509G>A GRCh37
NC_000003.10:g.33113513G>A NCBI36
NG_009005.1:g.5186C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307363.10:c.69C>T (GLB1) MANE Select ENSP00000306920.4:p.Gly23=
ENST00000342462.5:c.-407C>T (TMPPE) MANE Select ENSP00000343398.4:n.-407C>T
ENST00000307363.9:c.69C>T (GLB1) ENSP00000306920.4:p.Gly23=
ENST00000307377.12:c.69C>T (GLB1) ENSP00000305920.8:p.Gly23=
ENST00000415454.1:c.69C>T (GLB1) ENSP00000411813.1:p.Gly23=
ENST00000436768.1:c.69C>T (GLB1) ENSP00000387989.1:p.Gly23=
ENST00000438227.1:c.69C>T (GLB1) ENSP00000401250.1:p.Gly23=
ENST00000440656.1:c.-155C>T (GLB1) ENSP00000411769.1:n.-155C>T
ENST00000464355.1:n.27C>T (GLB1)
ENST00000482097.5:n.102C>T (GLB1)
ENST00000485698.5:n.130C>T (GLB1)
ENST00000498537.5:n.126C>T (GLB1)
NM_000404.2:c.69C>T (GLB1) NP_000395.2:p.Gly23=
NM_000404.3:c.69C>T (GLB1) NP_000395.2:p.Gly23=
NM_001135602.1:c.69C>T (GLB1) NP_001129074.1:p.Gly23=
NM_001135602.2:c.69C>T (GLB1) NP_001129074.1:p.Gly23=
NM_001317040.1:c.69C>T (GLB1) NP_001303969.1:p.Gly23=
NM_000404.4:c.69C>T (GLB1) MANE Select NP_000395.3:p.Gly23=
NM_001039770.3:c.-407C>T (TMPPE) MANE Select NP_001034859.2:n.-407C>T
NM_001136238.2:c.-303C>T (TMPPE) NP_001129710.1:n.-303C>T
NM_001135602.3:c.69C>T (GLB1) NP_001129074.2:p.Gly23=
NM_001317040.2:c.69C>T (GLB1) NP_001303969.2:p.Gly23=
NM_001393580.1:c.69C>T (GLB1) NP_001380509.1:p.Gly23=