Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8009531T>C , CM000679.2:g.8009531T>C | GRCh38 |
| NC_000017.10:g.7912849T>C , CM000679.1:g.7912849T>C | GRCh37 |
| NC_000017.9:g.7853574T>C | NCBI36 |
| NG_009092.1:g.11862T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000180.4:c.1694T>C MANE Select | NP_000171.1:p.Phe565Ser |
| ENST00000254854.5:c.1694T>C MANE Select | ENSP00000254854.4:p.Phe565Ser |
| NM_000180.3:c.1694T>C | NP_000171.1:p.Phe565Ser |
| ENST00000254854.4:c.1694T>C | ENSP00000254854.4:p.Phe565Ser |
| XM_011523816.1:c.1694T>C | XP_011522118.1:p.Phe565Ser |