Linked Data
MyVariant Identifiers:
chr1:g.1168018G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.1232638G>C , CM000663.2:g.1232638G>C | GRCh38 |
| NC_000001.10:g.1168018G>C , CM000663.1:g.1168018G>C | GRCh37 |
| NC_000001.9:g.1157881G>C | NCBI36 |
| NG_030007.1:g.4430C>G | |
| NG_033265.1:g.5390G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379198.5:c.360G>C MANE Select | ENSP00000368496.2:p.Leu120= | |
| ENST00000379198.3:c.360G>C | ENSP00000368496.2:p.Leu120= | |
| NM_080605.3:c.360G>C | NP_542172.2:p.Leu120= | |
| NM_080605.4:c.360G>C MANE Select | NP_542172.2:p.Leu120= |