HGVS | Genome Assembly |
---|---|
NC_000008.11:g.96145085G>C , CM000670.2:g.96145085G>C | GRCh38 |
NC_000008.10:g.97157313G>C , CM000670.1:g.97157313G>C | GRCh37 |
NC_000008.9:g.97226489G>C | NCBI36 |
NG_008981.1:g.20708C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000287020.7:c.846C>G MANE Select | ENSP00000287020.4:p.Thr282= | |
ENST00000287020.6:c.846C>G | ENSP00000287020.4:p.Thr282= | |
ENST00000620978.1:c.784C>G | ENSP00000480170.1:p.Gln262Glu | |
ENST00000621429.1:c.846C>G | ENSP00000483711.1:p.Thr282= | |
NM_001001557.2:c.846C>G | NP_001001557.1:p.Thr282= | |
XM_011517030.1:c.447C>G | XP_011515332.1:p.Thr149= | |
NM_001001557.3:c.846C>G | NP_001001557.1:p.Thr282= | |
NM_001001557.4:c.846C>G MANE Select | NP_001001557.1:p.Thr282= |