HGVS | Genome Assembly |
---|---|
NC_000007.14:g.93103903A>C , CM000669.2:g.93103903A>C | GRCh38 |
NC_000007.13:g.92733216A>C , CM000669.1:g.92733216A>C | GRCh37 |
NC_000007.12:g.92571152A>C | NCBI36 |
NG_023419.1:g.19121T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000379958.3:c.2195T>G MANE Select | ENSP00000369292.2:p.Ile732Ser | |
ENST00000379958.2:c.2195T>G | ENSP00000369292.2:p.Ile732Ser | |
ENST00000446617.1:c.2195T>G | ENSP00000414529.1:p.Ile732Ser | |
ENST00000620985.4:c.2195T>G | ENSP00000484636.1:p.Ile732Ser | |
NM_001193307.1:c.2195T>G | NP_001180236.1:p.Ile732Ser | |
NM_017654.3:c.2195T>G | NP_060124.2:p.Ile732Ser | |
NM_017654.4:c.2195T>G MANE Select | NP_060124.2:p.Ile732Ser | |
NM_001193307.2:c.2195T>G | NP_001180236.1:p.Ile732Ser |