MyVariant.info:
GRCh37
chr1:g.115220540A>G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.114677919A>G , CM000663.2:g.114677919A>G | GRCh38 |
| NC_000001.10:g.115220540A>G , CM000663.1:g.115220540A>G | GRCh37 |
| NC_000001.9:g.115022063A>G | NCBI36 |
| NG_008012.1:g.22637T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369538.4:c.1203T>C | ENSP00000358551.4:p.Thr401= | |
| ENST00000520113.7:c.1215T>C MANE Select | ENSP00000430075.3:p.Thr405= | |
| ENST00000637080.1:c.998T>C | ENSP00000489753.1:n.998T>C | |
| ENST00000639077.1:n.880T>C | ||
| ENST00000369538.3:c.1302T>C | ENSP00000358551.3:p.Thr434= | |
| ENST00000520113.6:c.1314T>C | ENSP00000430075.2:p.Thr438= | |
| NM_000036.2:c.1314T>C | NP_000027.2:p.Thr438= | |
| NM_001172626.1:c.1302T>C | NP_001166097.1:p.Thr434= | |
| NM_000036.3:c.1215T>C MANE Select | NP_000027.3:p.Thr405= | |
| NM_001172626.2:c.1203T>C | NP_001166097.2:p.Thr401= |