Linked Data
MyVariant Identifiers:
chr1:g.55464899C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.54999226C>T , CM000663.2:g.54999226C>T | GRCh38 |
| NC_000001.10:g.55464899C>T , CM000663.1:g.55464899C>T | GRCh37 |
| NC_000001.9:g.55237487C>T | NCBI36 |
| NG_008965.1:g.5283C>T | |
| NG_008965.2:g.5294C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651561.1:c.40C>T MANE Select | ENSP00000498282.1:p.Leu14= | |
| ENST00000371265.4:c.40C>T | ENSP00000360312.4:p.Leu14= | |
| NM_057176.2:c.40C>T | NP_476517.1:p.Leu14= | |
| NM_057176.3:c.40C>T MANE Select | NP_476517.1:p.Leu14= |