HGVS | Genome Assembly |
---|---|
NC_000008.11:g.10612841T>G , CM000670.2:g.10612841T>G | GRCh38 |
NC_000008.10:g.10470351T>G , CM000670.1:g.10470351T>G | GRCh37 |
NC_000008.9:g.10507761T>G | NCBI36 |
NG_028035.1:g.47267A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382483.4:c.1257A>C MANE Select | ENSP00000371923.3:p.Arg419Ser | |
ENST00000382483.3:c.1257A>C | ENSP00000371923.3:p.Arg419Ser | |
NM_178857.5:c.1257A>C | NP_849188.4:p.Arg419Ser | |
NM_178857.6:c.1257A>C MANE Select | NP_849188.4:p.Arg419Ser |