HGVS | Genome Assembly |
---|---|
NC_000008.11:g.96144665G>T , CM000670.2:g.96144665G>T | GRCh38 |
NC_000008.10:g.97156893G>T , CM000670.1:g.97156893G>T | GRCh37 |
NC_000008.9:g.97226069G>T | NCBI36 |
NG_008981.1:g.21128C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000287020.7:c.1266C>A MANE Select | ENSP00000287020.4:p.Pro422= | |
ENST00000287020.6:c.1266C>A | ENSP00000287020.4:p.Pro422= | |
ENST00000620978.1:c.806C>A | ENSP00000480170.1:p.Pro269Gln | |
ENST00000621429.1:c.1015C>A | ENSP00000483711.1:p.His339Asn | |
NM_001001557.2:c.1266C>A | NP_001001557.1:p.Pro422= | |
XM_011517030.1:c.867C>A | XP_011515332.1:p.Pro289= | |
NM_001001557.3:c.1266C>A | NP_001001557.1:p.Pro422= | |
NM_001001557.4:c.1266C>A MANE Select | NP_001001557.1:p.Pro422= |