Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.74685276C>T , CM000667.2:g.74685276C>T | GRCh38 |
| NC_000005.9:g.73981101C>T , CM000667.1:g.73981101C>T | GRCh37 |
| NC_000005.8:g.74016857C>T | NCBI36 |
| NG_009770.1:g.5133C>T | |
| NG_009770.2:g.50254C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000521.4:c.16C>T MANE Select | NP_000512.2:p.Leu6= |
| ENST00000261416.12:c.16C>T MANE Select | ENSP00000261416.7:p.Leu6= |
| NM_000521.3:c.16C>T | NP_000512.1:p.Leu6= |
| NM_001292004.1:c.-376-4052C>T | NP_001278933.1:n.-376-4052C>T |
| NM_001292004.2:c.-376-4052C>T | NP_001278933.1:n.-376-4052C>T |
| ENST00000261416.11:c.16C>T | ENSP00000261416.7:p.Leu6= |
| ENST00000511181.5:c.-376-4052C>T | ENSP00000426285.1:n.-376-4052C>T |
| ENST00000513079.5:n.81C>T | |
| ENST00000515528.1:n.71C>T |