HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154860565G>T , CM000685.2:g.154860565G>T | GRCh38 |
NC_000023.10:g.154088840G>T , CM000685.1:g.154088840G>T | GRCh37 |
NC_000023.9:g.153742034G>T | NCBI36 |
NG_011403.1:g.167159C>A | |
NG_011403.2:g.167159C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.6767C>A MANE Select | ENSP00000353393.4:p.Thr2256Lys | |
ENST00000644698.1:c.500C>A | ENSP00000495706.1:p.Thr167Lys | |
ENST00000330287.10:c.362C>A | ENSP00000327895.6:p.Thr121Lys | |
ENST00000360256.8:c.6767C>A | ENSP00000353393.4:p.Thr2256Lys | |
NM_000132.3:c.6767C>A | NP_000123.1:p.Thr2256Lys | |
NM_019863.2:c.362C>A | NP_063916.1:p.Thr121Lys | |
XM_011531126.1:c.6662C>A | XP_011529428.1:p.Thr2221Lys | |
NM_000132.4:c.6767C>A MANE Select | NP_000123.1:p.Thr2256Lys | |
NM_019863.3:c.362C>A | NP_063916.1:p.Thr121Lys |