Linked Data
MyVariant Identifiers:
chrX:g.119760632A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.120626777A>G , CM000685.2:g.120626777A>G | GRCh38 |
| NC_000023.10:g.119760632A>G , CM000685.1:g.119760632A>G | GRCh37 |
| NC_000023.9:g.119644660A>G | NCBI36 |
| NG_016219.1:g.8374T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000304661.6:c.390T>C MANE Select | ENSP00000304364.5:p.Phe130= | |
| ENST00000304661.5:c.390T>C | ENSP00000304364.5:p.Phe130= | |
| ENST00000371313.2:c.390T>C | ENSP00000360363.2:p.Phe130= | |
| NM_001011551.2:c.390T>C | NP_001011551.1:p.Phe130= | |
| NM_152692.4:c.390T>C | NP_689905.1:p.Phe130= | |
| NM_001011551.3:c.390T>C MANE Select | NP_001011551.1:p.Phe130= | |
| NM_152692.5:c.390T>C | NP_689905.1:p.Phe130= |