Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128278780A>G , CM000667.2:g.128278780A>G | GRCh38 |
| NC_000005.9:g.127614472A>G , CM000667.1:g.127614472A>G | GRCh37 |
| NC_000005.8:g.127642371A>G | NCBI36 |
| NG_008750.1:g.264264T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703783.1:n.3984T>C | ||
| ENST00000262464.9:c.7200T>C MANE Select | ENSP00000262464.4:p.Ser2400= | |
| ENST00000262464.8:c.7200T>C | ENSP00000262464.4:p.Ser2400= | |
| ENST00000508053.5:c.7200T>C | ENSP00000424571.1:p.Ser2400= | |
| ENST00000619499.4:c.7197T>C | ENSP00000482132.1:p.Ser2399= | |
| NM_001999.3:c.7200T>C | NP_001990.2:p.Ser2400= | |
| XM_017009228.2:c.7047T>C | XP_016864717.1:p.Ser2349= | |
| NM_001999.4:c.7200T>C MANE Select | NP_001990.2:p.Ser2400= |