HGVS | Genome Assembly |
---|---|
NC_000002.12:g.102452190C= , CM000664.2:g.102452190C= | GRCh38 |
NC_000002.11:g.103068650C= , CM000664.1:g.103068650C= | GRCh37 |
NC_000002.10:g.102435082C= | NCBI36 |
NG_011481.1:g.38397C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000687160.1:c.*9C= MANE Select | ENSP00000510345.1:n.*9C= | |
ENST00000264260.6:c.*9C= | ENSP00000264260.2:n.*9C= | |
ENST00000409369.1:c.*9C= | ENSP00000387201.1:n.*9C= | |
NM_003853.3:c.*9C= | NP_003844.1:n.*9C= | |
XM_011512087.1:c.*9C= | XP_011510389.1:n.*9C= | |
XM_011512088.1:c.*9C= | XP_011510390.1:n.*9C= | |
XM_011512087.2:c.*9C= | XP_011510389.1:n.*9C= | |
XM_011512088.2:c.*9C= | XP_011510390.1:n.*9C= | |
XM_017005173.1:c.*9C= | XP_016860662.1:n.*9C= | |
XM_024453197.1:c.*9C= | XP_024308965.1:n.*9C= | |
XM_024453198.1:c.*9C= | XP_024308966.1:n.*9C= | |
XM_024453199.1:c.*9C= | XP_024308967.1:n.*9C= | |
XM_024453200.1:c.*9C= | XP_024308968.1:n.*9C= | |
XM_024453201.1:c.*9C= | XP_024308969.1:n.*9C= | |
NM_001393486.1:c.*9C= | NP_001380415.1:n.*9C= | |
NM_001393487.1:c.*9C= MANE Select | NP_001380416.1:n.*9C= | |
NM_001393488.1:c.*9C= | NP_001380417.1:n.*9C= | |
NM_001393489.1:c.*9C= | NP_001380418.1:n.*9C= | |
NM_003853.4:c.*9C= | NP_003844.1:n.*9C= |