HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154860545T>A , CM000685.2:g.154860545T>A | GRCh38 |
NC_000023.10:g.154088820T>A , CM000685.1:g.154088820T>A | GRCh37 |
NC_000023.9:g.153742014T>A | NCBI36 |
NG_011403.1:g.167179A>T | |
NG_011403.2:g.167179A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000360256.9:c.6787A>T MANE Select | ENSP00000353393.4:p.Thr2263Ser | |
ENST00000644698.1:c.520A>T | ENSP00000495706.1:p.Thr174Ser | |
ENST00000330287.10:c.382A>T | ENSP00000327895.6:p.Thr128Ser | |
ENST00000360256.8:c.6787A>T | ENSP00000353393.4:p.Thr2263Ser | |
NM_000132.3:c.6787A>T | NP_000123.1:p.Thr2263Ser | |
NM_019863.2:c.382A>T | NP_063916.1:p.Thr128Ser | |
XM_011531126.1:c.6682A>T | XP_011529428.1:p.Thr2228Ser | |
NM_000132.4:c.6787A>T MANE Select | NP_000123.1:p.Thr2263Ser | |
NM_019863.3:c.382A>T | NP_063916.1:p.Thr128Ser |