Linked Data
ClinVar Variation Id:
1975714
ClinVar RCV Id:
RCV002746729
MyVariant Identifiers:
chr9:g.104188858G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.101426576G>A , CM000671.2:g.101426576G>A | GRCh38 |
| NC_000009.11:g.104188858G>A , CM000671.1:g.104188858G>A | GRCh37 |
| NC_000009.10:g.103228679G>A | NCBI36 |
| NG_012387.1:g.14205C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647789.2:c.603C>T MANE Select | ENSP00000497767.1:p.His201= | |
| ENST00000648064.1:c.603C>T | ENSP00000497990.1:p.His201= | |
| ENST00000648758.1:c.603C>T | ENSP00000497731.1:p.His201= | |
| ENST00000649902.1:c.603C>T | ENSP00000497216.1:p.His201= | |
| ENST00000374855.8:c.603C>T | ENSP00000363988.4:p.His201= | |
| ENST00000468981.3:n.130C>T | ||
| ENST00000616752.1:c.603C>T | ENSP00000481363.1:p.His201= | |
| NM_000035.3:c.603C>T | NP_000026.2:p.His201= | |
| NM_000035.4:c.603C>T MANE Select | NP_000026.2:p.His201= |