Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.88804542C>T , CM000678.2:g.88804542C>T | GRCh38 |
| NC_000016.9:g.88870950C>T , CM000678.1:g.88870950C>T | GRCh37 |
| NC_000016.8:g.87398451C>T | NCBI36 |
| NG_028266.1:g.5765C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_030928.4:c.229-3C>T MANE Select | NP_112190.2:n.229-3C>T |
| ENST00000301019.9:c.229-3C>T MANE Select | ENSP00000301019.4:n.229-3C>T |
| NM_030928.3:c.229-3C>T | NP_112190.2:n.229-3C>T |
| ENST00000301019.8:c.229-3C>T | ENSP00000301019.4:n.229-3C>T |