HGVS | Genome Assembly |
---|---|
NC_000010.11:g.52772275A= , CM000672.2:g.52772275A= | GRCh38 |
NC_000010.10:g.54532035A= , CM000672.1:g.54532035A= | GRCh37 |
NC_000010.9:g.54202041A= | NCBI36 |
NG_008196.1:g.4426T= , LRG_154:g.4426T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000674931.1:c.-10+462T= MANE Select | ENSP00000502789.1:n.-10+462T= | |
ENST00000675947.1:c.-25+462T= | ENSP00000502615.1:n.-25+462T= | |
XM_006717861.2:c.-25+462T= | XP_006717924.1:n.-25+462T= | |
XM_011539816.1:c.-10+462T= | XP_011538118.1:n.-10+462T= | |
XM_006717861.4:c.-25+462T= | XP_006717924.1:n.-25+462T= | |
XM_011539816.3:c.-10+462T= | XP_011538118.1:n.-10+462T= | |
NM_001378373.1:c.-10+462T= MANE Select | NP_001365302.1:n.-10+462T= | |
NM_001378374.1:c.-25+462T= | NP_001365303.1:n.-25+462T= |