HGVS | Genome Assembly |
---|---|
NC_000011.10:g.10763756A>T , CM000673.2:g.10763756A>T | GRCh38 |
NC_000011.9:g.10785303A>T , CM000673.1:g.10785303A>T | GRCh37 |
NC_000011.8:g.10741879A>T | NCBI36 |
NG_051671.1:g.17770A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361367.7:c.1071A>T MANE Select | ENSP00000355013.2:p.Lys357Asn | |
ENST00000361367.6:c.1071A>T | ENSP00000355013.2:p.Lys357Asn | |
NM_014633.4:c.1071A>T | NP_055448.1:p.Lys357Asn | |
NM_001346279.1:c.1071A>T | NP_001333208.1:p.Lys357Asn | |
NM_014633.5:c.1071A>T MANE Select | NP_055448.1:p.Lys357Asn | |
NM_001346279.2:c.1071A>T | NP_001333208.1:p.Lys357Asn |