Linked Data
ClinVar Variation Id:
2253646
ClinVar RCV Id:
RCV002758110
dbSNP Id:
rs901960857
gnomAD v3:
19-35849028-G-T
gnomAD v4:
19-35849028-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.35849028G>T , CM000681.2:g.35849028G>T | GRCh38 |
| NC_000019.9:g.36339930G>T , CM000681.1:g.36339930G>T | GRCh37 |
| NC_000019.8:g.41031770G>T | NCBI36 |
| NG_013356.2:g.25260C>A , LRG_693:g.25260C>A | |
| NG_051206.1:g.2394G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378910.10:c.960C>A MANE Select | ENSP00000368190.4:p.His320Gln | |
| ENST00000353632.6:c.960C>A | ENSP00000343634.5:p.His320Gln | |
| ENST00000378910.9:c.960C>A | ENSP00000368190.4:p.His320Gln | |
| NM_004646.3:c.960C>A , LRG_693t1:c.960C>A | NP_004637.1:p.His320Gln | |
| NM_004646.4:c.960C>A MANE Select | NP_004637.1:p.His320Gln |