HGVS | Genome Assembly |
---|---|
NC_000020.11:g.10658594A= , CM000682.2:g.10658594A= | GRCh38 |
NC_000020.10:g.10639242A= , CM000682.1:g.10639242A= | GRCh37 |
NC_000020.9:g.10587242A= | NCBI36 |
NG_007496.1:g.20453T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000254958.10:c.568T= MANE Select | ENSP00000254958.4:p.Tyr190= | |
ENST00000254958.9:c.568T= | ENSP00000254958.4:p.Tyr190= | |
ENST00000423891.6:n.434T= | ||
NM_000214.2:c.568T= | NP_000205.1:p.Tyr190= | |
NM_000214.3:c.568T= MANE Select | NP_000205.1:p.Tyr190= |