Linked Data
ClinVar Variation Id:
358694
dbSNP Id:
rs772860611
ExAC:
7:116436079 C / T
gnomAD v2:
7-116436079-C-T
gnomAD v4:
7-116796025-C-T
COSMIC:
COSM6454424
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.116796025C>T , CM000669.2:g.116796025C>T | GRCh38 |
| NC_000007.13:g.116436079C>T , CM000669.1:g.116436079C>T | GRCh37 |
| NC_000007.12:g.116223315C>T | NCBI36 |
| NG_008996.1:g.128621C>T , LRG_662:g.128621C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000436117.3:c.*1679C>T | ENSP00000410980.2:n.*1679C>T | |
| ENST00000318493.11:c.4128C>T | ENSP00000317272.6:p.Asn1376= | |
| ENST00000397752.8:c.4074C>T MANE Select | ENSP00000380860.3:p.Asn1358= | |
| ENST00000318493.10:c.4128C>T | ENSP00000317272.6:p.Asn1376= | |
| ENST00000397752.7:c.4074C>T | ENSP00000380860.3:p.Asn1358= | |
| NM_000245.2:c.4074C>T | NP_000236.2:p.Asn1358= | |
| NM_001127500.1:c.4128C>T , LRG_662t1:c.4128C>T | NP_001120972.1:p.Asn1376= | |
| XM_006715990.2:c.2784C>T | XP_006716053.1:p.Asn928= | |
| XM_006715991.2:c.2784C>T | XP_006716054.1:p.Asn928= | |
| XM_011516223.1:c.4131C>T | XP_011514525.1:p.Asn1377= | |
| NM_000245.3:c.4074C>T | NP_000236.2:p.Asn1358= | |
| NM_001127500.2:c.4128C>T | NP_001120972.1:p.Asn1376= | |
| NM_001324402.1:c.2784C>T | NP_001311331.1:p.Asn928= | |
| XR_001744772.1:n.4205C>T | ||
| NM_001127500.3:c.4128C>T | NP_001120972.1:p.Asn1376= | |
| NM_000245.4:c.4074C>T MANE Select | NP_000236.2:p.Asn1358= | |
| NM_001324402.2:c.2784C>T | NP_001311331.1:p.Asn928= |