Linked Data
ClinVar Variation Id:
1460828
ClinVar RCV Id:
RCV001983166
dbSNP Id:
rs2146023474
gnomAD v4:
19-7527549-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7527549C>T , CM000681.2:g.7527549C>T | GRCh38 |
| NC_000019.9:g.7592435C>T , CM000681.1:g.7592435C>T | GRCh37 |
| NC_000019.8:g.7498435C>T | NCBI36 |
| NG_015806.1:g.9940C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264079.11:c.601C>T MANE Select | ENSP00000264079.5:p.Pro201Ser | |
| ENST00000264079.10:c.601C>T | ENSP00000264079.5:p.Pro201Ser | |
| ENST00000394321.9:n.681C>T | ||
| ENST00000598406.1:n.422C>T | ||
| ENST00000601003.1:c.572-315C>T | ENSP00000469074.1:n.572-315C>T | |
| NM_020533.2:c.601C>T | NP_065394.1:p.Pro201Ser | |
| NM_020533.3:c.601C>T MANE Select | NP_065394.1:p.Pro201Ser |