Linked Data
MyVariant Identifiers:
chr1:g.215848866T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215675524T>G , CM000663.2:g.215675524T>G | GRCh38 |
| NC_000001.10:g.215848866T>G , CM000663.1:g.215848866T>G | GRCh37 |
| NC_000001.9:g.213915489T>G | NCBI36 |
| NG_009497.1:g.752873A>C | |
| NG_009497.2:g.752925A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.12387A>C MANE Select | ENSP00000305941.3:p.Thr4129= | |
| ENST00000674083.1:c.12387A>C | ENSP00000501296.1:p.Thr4129= | |
| ENST00000307340.7:c.12387A>C | ENSP00000305941.3:p.Thr4129= | |
| NM_206933.2:c.12387A>C | NP_996816.2:p.Thr4129= | |
| NM_206933.3:c.12387A>C | NP_996816.2:p.Thr4129= | |
| NM_206933.4:c.12387A>C MANE Select | NP_996816.3:p.Thr4129= |