Canonical Allele Identifier: CA432953803
Gene: GLB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.33063147A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33021655A>G , CM000665.2:g.33021655A>G GRCh38
NC_000003.11:g.33063147A>G , CM000665.1:g.33063147A>G GRCh37
NC_000003.10:g.33038151A>G NCBI36
NG_009005.1:g.80548T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307363.10:c.1144T>C MANE Select ENSP00000306920.4:p.Leu382=
ENST00000307363.9:c.1144T>C ENSP00000306920.4:p.Leu382=
ENST00000307377.12:c.751T>C ENSP00000305920.8:p.Leu251=
ENST00000399402.7:c.1054T>C ENSP00000382333.2:p.Leu352=
ENST00000461475.5:n.243T>C
ENST00000467571.5:n.181T>C
ENST00000473477.1:n.176T>C
ENST00000482097.5:n.519T>C
ENST00000497796.5:n.396T>C
NM_000404.2:c.1144T>C NP_000395.2:p.Leu382=
NM_000404.3:c.1144T>C NP_000395.2:p.Leu382=
NM_001079811.1:c.1054T>C NP_001073279.1:p.Leu352=
NM_001079811.2:c.1054T>C NP_001073279.1:p.Leu352=
NM_001135602.1:c.751T>C NP_001129074.1:p.Leu251=
NM_001135602.2:c.751T>C NP_001129074.1:p.Leu251=
NM_001317040.1:c.1288T>C NP_001303969.1:p.Leu430=
XR_001740634.1:n.1543-533A>G
NM_000404.4:c.1144T>C MANE Select NP_000395.3:p.Leu382=
NM_001079811.3:c.1054T>C NP_001073279.2:p.Leu352=
NM_001135602.3:c.751T>C NP_001129074.2:p.Leu251=
NM_001317040.2:c.1288T>C NP_001303969.2:p.Leu430=
NM_001393580.1:c.1144T>C NP_001380509.1:p.Leu382=