Linked Data
ClinVar Variation Id:
323299
dbSNP Id:
rs200715586
ExAC:
17:40695296 C / T
gnomAD v2:
17-40695296-C-T
gnomAD v3:
17-42543278-C-T
gnomAD v4:
17-42543278-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42543278C>T , CM000679.2:g.42543278C>T | GRCh38 |
| NC_000017.10:g.40695296C>T , CM000679.1:g.40695296C>T | GRCh37 |
| NC_000017.9:g.37948822C>T | NCBI36 |
| NG_011552.1:g.12346C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225927.7:c.1272C>T MANE Select | ENSP00000225927.1:p.Asn424= | |
| ENST00000225927.6:c.1272C>T | ENSP00000225927.1:p.Asn424= | |
| ENST00000591587.1:c.610C>T | ENSP00000467836.1:n.610C>T | |
| ENST00000592454.1:c.311C>T | ||
| NM_000263.3:c.1272C>T | NP_000254.2:p.Asn424= | |
| XM_006721920.2:c.441C>T | XP_006721983.1:p.Asn147= | |
| XM_011524840.1:c.273C>T | XP_011523142.1:p.Asn91= | |
| XM_017024687.1:c.441C>T | XP_016880176.1:p.Asn147= | |
| XM_024450771.1:c.1329C>T | XP_024306539.1:p.Asn443= | |
| XM_024450772.1:c.273C>T | XP_024306540.1:p.Asn91= | |
| NM_000263.4:c.1272C>T MANE Select | NP_000254.2:p.Asn424= |