HGVS | Genome Assembly |
---|---|
NC_000011.10:g.2445432A>G , CM000673.2:g.2445432A>G | GRCh38 |
NC_000011.9:g.2466662A>G , CM000673.1:g.2466662A>G | GRCh37 |
NC_000011.8:g.2423238A>G | NCBI36 |
NG_008935.1:g.5442A>G , LRG_287:g.5442A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000496887.7:c.73A>G | ENSP00000434560.2:p.Asn25Asp | |
ENST00000646564.2:c.334A>G | ENSP00000495806.2:p.Asn112Asp | |
ENST00000155840.12:c.334A>G MANE Select | ENSP00000155840.2:p.Asn112Asp | |
ENST00000155840.9:c.334A>G | ENSP00000155840.2:p.Asn112Asp | |
ENST00000345015.4:n.111A>G | ||
ENST00000496887.6:c.73A>G | ENSP00000434560.1:p.Asn25Asp | |
NM_000218.2:c.334A>G , LRG_287t1:c.334A>G | NP_000209.2:p.Asn112Asp | |
NM_000218.3:c.334A>G MANE Select | NP_000209.2:p.Asn112Asp |