HGVS | Genome Assembly |
---|---|
NC_000004.12:g.46123867C>G , CM000666.2:g.46123867C>G | GRCh38 |
NC_000004.11:g.46125884C>G , CM000666.1:g.46125884C>G | GRCh37 |
NC_000004.10:g.45820641C>G | NCBI36 |
NG_046964.1:g.5199G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295452.5:c.47G>C MANE Select | ENSP00000295452.4:p.Ser16Thr | |
ENST00000295452.4:c.47G>C | ENSP00000295452.4:p.Ser16Thr | |
NM_173536.3:c.47G>C | NP_775807.2:p.Ser16Thr | |
NM_173536.4:c.47G>C MANE Select | NP_775807.2:p.Ser16Thr |