Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.31666484T>C , CM000683.2:g.31666484T>C | GRCh38 |
| NC_000021.8:g.33038797T>C , CM000683.1:g.33038797T>C | GRCh37 |
| NC_000021.7:g.31960668T>C | NCBI36 |
| NG_008689.1:g.11863T>C , LRG_652:g.11863T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000454.5:c.205T>C MANE Select | NP_000445.1:p.Ser69Pro |
| ENST00000270142.11:c.205T>C MANE Select | ENSP00000270142.7:p.Ser69Pro |
| NM_000454.4:c.205T>C , LRG_652t1:c.205T>C | NP_000445.1:p.Ser69Pro |
| ENST00000270142.10:c.205T>C | ENSP00000270142.6:p.Ser69Pro |
| ENST00000389995.4:c.148T>C | ENSP00000374645.4:p.Ser50Pro |
| ENST00000470944.1:n.1133T>C | |
| ENST00000476106.5:n.468T>C |