Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.25007070A>G , CM000685.2:g.25007070A>G | GRCh38 |
| NC_000023.10:g.25025187A>G , CM000685.1:g.25025187A>G | GRCh37 |
| NC_000023.9:g.24935108A>G | NCBI36 |
| NG_008281.1:g.13879T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379044.5:c.1448+41T>C MANE Select | ENSP00000368332.4:n.1448+41T>C | |
| ENST00000637993.1:c.61+41T>C | ||
| ENST00000379044.4:c.1448+41T>C | ENSP00000368332.4:n.1448+41T>C | |
| NM_139058.2:c.1448+41T>C | NP_620689.1:n.1448+41T>C | |
| NM_139058.3:c.1448+41T>C MANE Select | NP_620689.1:n.1448+41T>C |