HGVS | Genome Assembly |
---|---|
NC_000007.14:g.93104132A>G , CM000669.2:g.93104132A>G | GRCh38 |
NC_000007.13:g.92733445A>G , CM000669.1:g.92733445A>G | GRCh37 |
NC_000007.12:g.92571381A>G | NCBI36 |
NG_023419.1:g.18892T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000379958.3:c.1966T>C MANE Select | ENSP00000369292.2:p.Cys656Arg | |
ENST00000379958.2:c.1966T>C | ENSP00000369292.2:p.Cys656Arg | |
ENST00000446617.1:c.1966T>C | ENSP00000414529.1:p.Cys656Arg | |
ENST00000620985.4:c.1966T>C | ENSP00000484636.1:p.Cys656Arg | |
NM_001193307.1:c.1966T>C | NP_001180236.1:p.Cys656Arg | |
NM_017654.3:c.1966T>C | NP_060124.2:p.Cys656Arg | |
NM_017654.4:c.1966T>C MANE Select | NP_060124.2:p.Cys656Arg | |
NM_001193307.2:c.1966T>C | NP_001180236.1:p.Cys656Arg |