HGVS | Genome Assembly |
---|---|
NC_000011.10:g.637527A>C , CM000673.2:g.637527A>C | GRCh38 |
NC_000011.9:g.637527A>C , CM000673.1:g.637527A>C | GRCh37 |
NC_000011.8:g.627527A>C | NCBI36 |
NG_021241.1:g.5223A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000176183.6:c.223A>C MANE Select | ENSP00000176183.5:p.Ser75Arg | |
ENST00000176183.5:c.223A>C | ENSP00000176183.5:p.Ser75Arg | |
NM_000797.3:c.223A>C | NP_000788.2:p.Ser75Arg | |
NM_000797.4:c.223A>C MANE Select | NP_000788.2:p.Ser75Arg |