Canonical Allele Identifier: CA352007434

Linked Data

dbSNP Id: rs889228362
gnomAD v3: 3-33097012-C-G
gnomAD v4: 3-33097012-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33097012C>G , CM000665.2:g.33097012C>G GRCh38
NC_000003.11:g.33138504C>G , CM000665.1:g.33138504C>G GRCh37
NC_000003.10:g.33113508C>G NCBI36
NG_009005.1:g.5191G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307363.10:c.74G>C (GLB1) MANE Select ENSP00000306920.4:p.Arg25Pro
ENST00000342462.5:c.-402G>C (TMPPE) MANE Select ENSP00000343398.4:n.-402G>C
ENST00000307363.9:c.74G>C (GLB1) ENSP00000306920.4:p.Arg25Pro
ENST00000307377.12:c.74G>C (GLB1) ENSP00000305920.8:p.Arg25Pro
ENST00000415454.1:c.74G>C (GLB1) ENSP00000411813.1:p.Arg25Pro
ENST00000436768.1:c.74G>C (GLB1) ENSP00000387989.1:p.Arg25Pro
ENST00000438227.1:c.74G>C (GLB1) ENSP00000401250.1:p.Arg25Pro
ENST00000440656.1:c.-150G>C (GLB1) ENSP00000411769.1:n.-150G>C
ENST00000464355.1:n.32G>C (GLB1)
ENST00000482097.5:n.107G>C (GLB1)
ENST00000485698.5:n.135G>C (GLB1)
ENST00000498537.5:n.131G>C (GLB1)
NM_000404.2:c.74G>C (GLB1) NP_000395.2:p.Arg25Pro
NM_000404.3:c.74G>C (GLB1) NP_000395.2:p.Arg25Pro
NM_001135602.1:c.74G>C (GLB1) NP_001129074.1:p.Arg25Pro
NM_001135602.2:c.74G>C (GLB1) NP_001129074.1:p.Arg25Pro
NM_001317040.1:c.74G>C (GLB1) NP_001303969.1:p.Arg25Pro
NM_000404.4:c.74G>C (GLB1) MANE Select NP_000395.3:p.Arg25Pro
NM_001039770.3:c.-402G>C (TMPPE) MANE Select NP_001034859.2:n.-402G>C
NM_001136238.2:c.-298G>C (TMPPE) NP_001129710.1:n.-298G>C
NM_001135602.3:c.74G>C (GLB1) NP_001129074.2:p.Arg25Pro
NM_001317040.2:c.74G>C (GLB1) NP_001303969.2:p.Arg25Pro
NM_001393580.1:c.74G>C (GLB1) NP_001380509.1:p.Arg25Pro