HGVS | Genome Assembly |
---|---|
NC_000010.11:g.102837531T>C , CM000672.2:g.102837531T>C | GRCh38 |
NC_000010.10:g.104597288T>C , CM000672.1:g.104597288T>C | GRCh37 |
NC_000010.9:g.104587278T>C | NCBI36 |
NG_007955.1:g.5003A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369887.3:c.-170A>G | ENSP00000358903.3:n.-170A>G | |
NM_000102.3:c.-170A>G | NP_000093.1:n.-170A>G |