Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.37804084T>C , CM000685.2:g.37804084T>C | GRCh38 |
| NC_000023.10:g.37663337T>C , CM000685.1:g.37663337T>C | GRCh37 |
| NC_000023.9:g.37548281T>C | NCBI36 |
| NG_009065.1:g.29068T>C , LRG_53:g.29068T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696170.1:c.*614T>C | ENSP00000512461.1:n.*614T>C | |
| ENST00000696171.1:c.1009T>C | ENSP00000512462.1:p.Cys337Arg | |
| ENST00000378588.5:c.1105T>C MANE Select | ENSP00000367851.4:p.Cys369Arg | |
| ENST00000378588.4:c.1105T>C | ENSP00000367851.4:p.Cys369Arg | |
| ENST00000465127.1:c.171+378084T>C | ENSP00000417050.1:n.171+378084T>C | |
| NM_000397.3:c.1105T>C , LRG_53t1:c.1105T>C | NP_000388.2:p.Cys369Arg | |
| XM_011543890.1:c.799T>C | XP_011542192.1:p.Cys267Arg | |
| NM_000397.4:c.1105T>C MANE Select | NP_000388.2:p.Cys369Arg |