HGVS | Genome Assembly |
---|---|
NC_000015.10:g.45480165A>G , CM000677.2:g.45480165A>G | GRCh38 |
NC_000015.9:g.45772363A>G , CM000677.1:g.45772363A>G | GRCh37 |
NC_000015.8:g.43559655A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261867.5:c.*4998T>C MANE Select | ENSP00000261867.3:n.*4998T>C | |
ENST00000261867.4:c.*4998T>C | ENSP00000261867.3:n.*4998T>C | |
NM_013309.5:c.*4998T>C | NP_037441.2:n.*4998T>C | |
NM_013309.6:c.*4998T>C MANE Select | NP_037441.2:n.*4998T>C |