HGVS | Genome Assembly |
---|---|
NC_000022.11:g.43163236T>C , CM000684.2:g.43163236T>C | GRCh38 |
NC_000022.10:g.43559242T>C , CM000684.1:g.43559242T>C | GRCh37 |
NC_000022.9:g.41889186T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000337554.8:c.*245T>C MANE Select | ENSP00000338004.3:n.*245T>C | |
ENST00000337554.7:c.*245T>C | ENSP00000338004.3:n.*245T>C | |
ENST00000396265.4:c.*245T>C | ENSP00000379563.4:n.*245T>C | |
ENST00000583777.5:c.*245T>C | ENSP00000463495.1:n.*245T>C | |
NM_000714.5:c.*245T>C | NP_000705.2:n.*245T>C | |
NM_001256530.1:c.*245T>C | NP_001243459.1:n.*245T>C | |
NM_001256531.1:c.*245T>C | NP_001243460.1:n.*245T>C | |
NR_046308.1:n.664T>C | ||
NM_000714.6:c.*245T>C MANE Select | NP_000705.2:n.*245T>C | |
NR_046308.2:n.619T>C |