Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.152648765A= , CM000669.2:g.152648765A= | GRCh38 |
| NC_000007.13:g.152345850A= , CM000669.1:g.152345850A= | GRCh37 |
| NC_000007.12:g.151976783A= | NCBI36 |
| NG_027988.1:g.32401T= | |
| NG_027988.2:g.32401T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698506.1:c.552T= | ENSP00000513758.1:p.Phe184= | |
| ENST00000359321.2:c.720T= MANE Select | ENSP00000352271.1:p.Phe240= | |
| ENST00000359321.1:c.720T= | ENSP00000352271.1:p.Phe240= | |
| ENST00000495707.1:n.742T= | ||
| NM_005431.1:c.720T= | NP_005422.1:p.Phe240= | |
| NM_005431.2:c.720T= MANE Select | NP_005422.1:p.Phe240= |