Linked Data
MyVariant Identifiers:
chr14:g.101200648G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.100734311G>C , CM000676.2:g.100734311G>C | GRCh38 |
| NC_000014.8:g.101200648G>C , CM000676.1:g.101200648G>C | GRCh37 |
| NC_000014.7:g.100270401G>C | NCBI36 |
| NG_016863.2:g.12447G>C | |
| NG_016863.3:g.12447G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000341267.9:c.567G>C MANE Select | ENSP00000340292.4:p.Gly189= | |
| ENST00000331224.10:c.567G>C | ENSP00000331081.6:p.Gly189= | |
| ENST00000341267.8:c.567G>C | ENSP00000340292.4:p.Gly189= | |
| NM_003836.5:c.567G>C | NP_003827.3:p.Gly189= | |
| NM_001317172.1:c.567G>C | NP_001304101.1:p.Gly189= | |
| NM_003836.6:c.567G>C | NP_003827.3:p.Gly189= | |
| NM_001317172.2:c.567G>C | NP_001304101.2:p.Gly189= | |
| NM_003836.7:c.567G>C MANE Select | NP_003827.4:p.Gly189= |