Canonical Allele Identifier: CA396897648
Gene: PLCG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81889175C>G , CM000678.2:g.81889175C>G GRCh38
NC_000016.9:g.81922780C>G , CM000678.1:g.81922780C>G GRCh37
NC_000016.8:g.80480281C>G NCBI36
NG_032019.2:g.155079C>G , LRG_376:g.155079C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000563193.2:c.769C>G ENSP00000455533.2:p.His257Asp
ENST00000697561.1:c.*198C>G ENSP00000513337.1:n.*198C>G
ENST00000697562.1:c.769C>G ENSP00000513338.1:p.His257Asp
ENST00000697563.1:c.*615C>G ENSP00000513339.1:n.*615C>G
ENST00000697564.1:c.652C>G ENSP00000513340.1:p.His218Asp
ENST00000697565.1:n.709C>G
ENST00000697581.1:c.*763C>G ENSP00000513346.1:n.*763C>G
ENST00000697582.1:c.769C>G ENSP00000513347.1:p.His257Asp
ENST00000697583.1:c.568C>G ENSP00000513349.1:p.His190Asp
ENST00000697584.1:c.568C>G ENSP00000513350.1:p.His190Asp
ENST00000697585.1:c.568C>G ENSP00000513351.1:p.His190Asp
ENST00000697586.1:c.568C>G ENSP00000513352.1:p.His190Asp
ENST00000697587.1:c.568C>G ENSP00000513353.1:p.His190Asp
ENST00000564138.6:c.769C>G MANE Select ENSP00000482457.1:p.His257Asp
ENST00000359376.7:c.769C>G ENSP00000352336.4:p.His257Asp
ENST00000563193.1:c.77C>G
ENST00000564138.5:c.769C>G ENSP00000482457.1:p.His257Asp
ENST00000567980.5:n.1013C>G
NM_002661.4:c.769C>G NP_002652.2:p.His257Asp
XM_011523108.1:c.883C>G XP_011521410.1:p.His295Asp
NM_002661.5:c.769C>G MANE Select NP_002652.2:p.His257Asp