HGVS | Genome Assembly |
---|---|
NC_000007.14:g.93104047_93104049del , CM000669.2:g.93104047_93104049del | GRCh38 |
NC_000007.13:g.92733360_92733362del , CM000669.1:g.92733360_92733362del | GRCh37 |
NC_000007.12:g.92571296_92571298del | NCBI36 |
NG_023419.1:g.18975_18977del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000379958.3:c.2049_2051del MANE Select | ENSP00000369292.2:p.Tyr684del | |
ENST00000379958.2:c.2049_2051del | ENSP00000369292.2:p.Tyr684del | |
ENST00000446617.1:c.2049_2051del | ENSP00000414529.1:p.Tyr684del | |
ENST00000620985.4:c.2049_2051del | ENSP00000484636.1:p.Tyr684del | |
NM_001193307.1:c.2049_2051del | NP_001180236.1:p.Tyr684del | |
NM_017654.3:c.2049_2051del | NP_060124.2:p.Tyr684del | |
NM_017654.4:c.2049_2051del MANE Select | NP_060124.2:p.Tyr684del | |
NM_001193307.2:c.2049_2051del | NP_001180236.1:p.Tyr684del |