Linked Data
MyVariant Identifiers:
chr13:g.52971725C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.52397590C>G , CM000675.2:g.52397590C>G | GRCh38 |
| NC_000013.10:g.52971725C>G , CM000675.1:g.52971725C>G | GRCh37 |
| NC_000013.9:g.51869726C>G | NCBI36 |
| NG_047168.1:g.13905G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258613.5:c.663G>C MANE Select | ENSP00000258613.4:p.Leu221= | |
| ENST00000648254.1:c.663G>C | ENSP00000497520.1:p.Leu221= | |
| ENST00000258613.4:c.663G>C | ENSP00000258613.4:p.Leu221= | |
| ENST00000349258.8:c.663G>C | ENSP00000340650.4:p.Leu221= | |
| NM_018676.3:c.663G>C | NP_061146.1:p.Leu221= | |
| NM_199263.2:c.663G>C | NP_954872.1:p.Leu221= | |
| NM_018676.4:c.663G>C MANE Select | NP_061146.1:p.Leu221= | |
| NM_199263.3:c.663G>C | NP_954872.1:p.Leu221= |