HGVS | Genome Assembly |
---|---|
NC_000008.11:g.10612891G>A , CM000670.2:g.10612891G>A | GRCh38 |
NC_000008.10:g.10470401G>A , CM000670.1:g.10470401G>A | GRCh37 |
NC_000008.9:g.10507811G>A | NCBI36 |
NG_028035.1:g.47217C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382483.4:c.1207C>T MANE Select | ENSP00000371923.3:p.Pro403Ser | |
ENST00000382483.3:c.1207C>T | ENSP00000371923.3:p.Pro403Ser | |
NM_178857.5:c.1207C>T | NP_849188.4:p.Pro403Ser | |
NM_178857.6:c.1207C>T MANE Select | NP_849188.4:p.Pro403Ser |