Linked Data
MyVariant Identifiers:
chr1:g.204159813G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.204190685G>C , CM000663.2:g.204190685G>C | GRCh38 |
| NC_000001.10:g.204159813G>C , CM000663.1:g.204159813G>C | GRCh37 |
| NC_000001.9:g.202426436G>C | NCBI36 |
| NG_032151.1:g.10807C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367194.5:c.216C>G MANE Select | ENSP00000356162.4:p.Ser72= | |
| ENST00000367194.4:c.216C>G | ENSP00000356162.4:p.Ser72= | |
| ENST00000625357.1:c.216C>G | ENSP00000485957.1:p.Ser72= | |
| NM_002256.3:c.216C>G | NP_002247.3:p.Ser72= | |
| XM_011509525.1:c.216C>G | XP_011507827.1:p.Ser72= | |
| NM_002256.4:c.216C>G MANE Select | NP_002247.3:p.Ser72= |