Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.52772210C= , CM000672.2:g.52772210C= | GRCh38 |
| NC_000010.10:g.54531970C= , CM000672.1:g.54531970C= | GRCh37 |
| NC_000010.9:g.54201976C= | NCBI36 |
| NG_008196.1:g.4491G= , LRG_154:g.4491G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000674931.1:c.-10+527G= MANE Select | ENSP00000502789.1:n.-10+527G= | |
| ENST00000675947.1:c.-25+527G= | ENSP00000502615.1:n.-25+527G= | |
| XM_006717861.2:c.-25+527G= | XP_006717924.1:n.-25+527G= | |
| XM_011539816.1:c.-10+527G= | XP_011538118.1:n.-10+527G= | |
| XM_006717861.4:c.-25+527G= | XP_006717924.1:n.-25+527G= | |
| XM_011539816.3:c.-10+527G= | XP_011538118.1:n.-10+527G= | |
| NM_001378373.1:c.-10+527G= MANE Select | NP_001365302.1:n.-10+527G= | |
| NM_001378374.1:c.-25+527G= | NP_001365303.1:n.-25+527G= |