HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154837687A>C , CM000685.2:g.154837687A>C | GRCh38 |
NC_000023.10:g.154065962A>C , CM000685.1:g.154065962A>C | GRCh37 |
NC_000023.9:g.153719156A>C | NCBI36 |
NG_011403.1:g.190037T>G | |
NG_033065.1:g.1976T>G | |
NG_011403.2:g.190037T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000360256.9:c.6966T>G MANE Select | ENSP00000353393.4:p.Thr2322= | |
ENST00000644698.1:c.699T>G | ENSP00000495706.1:p.Thr233= | |
ENST00000330287.10:c.561T>G | ENSP00000327895.6:p.Thr187= | |
ENST00000360256.8:c.6966T>G | ENSP00000353393.4:p.Thr2322= | |
NM_000132.3:c.6966T>G | NP_000123.1:p.Thr2322= | |
NM_019863.2:c.561T>G | NP_063916.1:p.Thr187= | |
XM_011531126.1:c.6861T>G | XP_011529428.1:p.Thr2287= | |
NM_000132.4:c.6966T>G MANE Select | NP_000123.1:p.Thr2322= | |
NM_019863.3:c.561T>G | NP_063916.1:p.Thr187= |