HGVS | Genome Assembly |
---|---|
NC_000008.11:g.18400851C= , CM000670.2:g.18400851C= | GRCh38 |
NC_000008.10:g.18258361C= , CM000670.1:g.18258361C= | GRCh37 |
NC_000008.9:g.18302641C= | NCBI36 |
NG_012246.1:g.14607C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000286479.4:c.848C= MANE Select | ENSP00000286479.3:p.Pro283= | |
ENST00000286479.3:c.848C= | ENSP00000286479.3:p.Pro283= | |
ENST00000520116.1:c.458C= | ENSP00000428416.1:p.Pro153= | |
NM_000015.2:c.848C= | NP_000006.2:p.Pro283= | |
XM_011544358.1:c.848C= | XP_011542660.1:p.Pro283= | |
XM_017012938.1:c.848C= | XP_016868427.1:p.Pro283= | |
NM_000015.3:c.848C= MANE Select | NP_000006.2:p.Pro283= |