Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86670956T>G , CM000670.2:g.86670956T>G | GRCh38 |
| NC_000008.10:g.87683184T>G , CM000670.1:g.87683184T>G | GRCh37 |
| NC_000008.9:g.87752300T>G | NCBI36 |
| NG_016980.1:g.77720A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320005.6:c.481A>C MANE Select | ENSP00000316605.5:p.Ser161Arg | |
| ENST00000680314.1:n.242A>C | ||
| ENST00000681746.1:c.481A>C | ENSP00000505959.1:p.Ser161Arg | |
| ENST00000320005.5:c.481A>C | ENSP00000316605.5:p.Ser161Arg | |
| NM_019098.4:c.481A>C | NP_061971.3:p.Ser161Arg | |
| XM_011517138.1:c.67A>C | XP_011515440.1:p.Ser23Arg | |
| XM_011517138.2:c.67A>C | XP_011515440.1:p.Ser23Arg | |
| NM_019098.5:c.481A>C MANE Select | NP_061971.3:p.Ser161Arg |