HGVS | Genome Assembly |
---|---|
NC_000011.10:g.202997A>G , CM000673.2:g.202997A>G | GRCh38 |
NC_000011.9:g.202997A>G , CM000673.1:g.202997A>G | GRCh37 |
NC_000011.8:g.192997A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382762.8:c.*2305T>C MANE Select | ENSP00000372210.3:n.*2305T>C | |
ENST00000325147.13:c.*2473T>C | ENSP00000339093.7:n.*2473T>C | |
ENST00000382762.7:c.*2305T>C | ENSP00000372210.3:n.*2305T>C | |
ENST00000410108.5:c.168+2614T>C | ENSP00000386558.1:n.168+2614T>C | |
NM_001098787.1:c.*2305T>C | NP_001092257.1:n.*2305T>C | |
NM_016526.4:c.*2473T>C | NP_057610.2:n.*2473T>C | |
NM_001098787.2:c.*2305T>C MANE Select | NP_001092257.1:n.*2305T>C | |
NM_016526.5:c.*2473T>C | NP_057610.2:n.*2473T>C |