dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32203298A>C , CM000668.2:g.32203298A>C | GRCh38 |
| NC_000006.11:g.32171075A>C , CM000668.1:g.32171075A>C | GRCh37 |
| NC_000006.10:g.32279053A>C | NCBI36 |
| NG_028190.1:g.25770T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375023.3:c.3231+472T>G MANE Select | ENSP00000364163.3:n.3231+472T>G | |
| ENST00000474612.1:n.619T>G | ||
| NM_004557.3:c.3231+472T>G | NP_004548.3:n.3231+472T>G | |
| NR_134949.1:n.3472+472T>G | ||
| NR_134950.1:n.3370+472T>G | ||
| NM_004557.4:c.3231+472T>G MANE Select | NP_004548.3:n.3231+472T>G | |
| NR_134949.2:n.3472+472T>G | ||
| NR_134950.2:n.3370+472T>G |