Linked Data
ClinVar Variation Id:
1360824
ClinVar RCV Id:
RCV001907209
dbSNP Id:
rs963470037
gnomAD v2:
7-143018861-T-C
gnomAD v3:
7-143321768-T-C
gnomAD v4:
7-143321768-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.143321768T>C , CM000669.2:g.143321768T>C | GRCh38 |
| NC_000007.13:g.143018861T>C , CM000669.1:g.143018861T>C | GRCh37 |
| NC_000007.12:g.142728983T>C | NCBI36 |
| NG_009815.1:g.10643T>C | |
| NG_009815.2:g.10643T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650516.2:c.616T>C | ENSP00000498052.2:p.Tyr206His | |
| ENST00000343257.7:c.616T>C MANE Select | ENSP00000339867.2:p.Tyr206His | |
| ENST00000432192.6:c.384T>C | ||
| ENST00000455478.6:c.70T>C | ENSP00000400027.2:p.Tyr24His | |
| ENST00000650516.1:c.616T>C | ENSP00000498052.1:p.Tyr206His | |
| ENST00000343257.6:c.616T>C | ENSP00000339867.2:p.Tyr206His | |
| ENST00000432192.5:c.74T>C | ||
| ENST00000455478.5:c.74T>C | ||
| ENST00000495612.1:n.74T>C | ||
| NM_000083.2:c.616T>C | NP_000074.2:p.Tyr206His | |
| NR_046453.1:n.703T>C | ||
| XM_011515781.1:c.616T>C | XP_011514083.1:p.Tyr206His | |
| XM_017011739.1:c.323T>C | XP_016867228.1:p.Ile108Thr | |
| XM_017011740.1:c.323T>C | XP_016867229.1:p.Ile108Thr | |
| NM_000083.3:c.616T>C MANE Select | NP_000074.3:p.Tyr206His | |
| NR_046453.2:n.718T>C |