Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.52772308T>G , CM000672.2:g.52772308T>G | GRCh38 |
| NC_000010.10:g.54532068T>G , CM000672.1:g.54532068T>G | GRCh37 |
| NC_000010.9:g.54202074T>G | NCBI36 |
| NG_008196.1:g.4393A>C , LRG_154:g.4393A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000674931.1:c.-10+429A>C MANE Select | ENSP00000502789.1:n.-10+429A>C | |
| ENST00000675947.1:c.-25+429A>C | ENSP00000502615.1:n.-25+429A>C | |
| XM_006717861.2:c.-25+429A>C | XP_006717924.1:n.-25+429A>C | |
| XM_011539816.1:c.-10+429A>C | XP_011538118.1:n.-10+429A>C | |
| XM_006717861.4:c.-25+429A>C | XP_006717924.1:n.-25+429A>C | |
| XM_011539816.3:c.-10+429A>C | XP_011538118.1:n.-10+429A>C | |
| NM_001378373.1:c.-10+429A>C MANE Select | NP_001365302.1:n.-10+429A>C | |
| NM_001378374.1:c.-25+429A>C | NP_001365303.1:n.-25+429A>C |