HGVS | Genome Assembly |
---|---|
NC_000023.11:g.47574019A>G , CM000685.2:g.47574019A>G | GRCh38 |
NC_000023.10:g.47433418A>G , CM000685.1:g.47433418A>G | GRCh37 |
NC_000023.9:g.47318362A>G | NCBI36 |
NG_008437.1:g.50839T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295987.13:c.1965T>C MANE Select | ENSP00000295987.7:p.Pro655= | |
ENST00000340666.5:c.1965T>C | ENSP00000343206.4:p.Pro655= | |
ENST00000640721.1:c.70+669T>C | ENSP00000492857.1:n.70+669T>C | |
ENST00000295987.11:c.1965T>C | ENSP00000295987.7:p.Pro655= | |
ENST00000340666.4:c.1965T>C | ENSP00000343206.4:p.Pro655= | |
NM_006950.3:c.1965T>C MANE Select | NP_008881.2:p.Pro655= | |
NM_133499.2:c.1965T>C | NP_598006.1:p.Pro655= |