Linked Data
dbSNP Id:
rs566180576
gnomAD v2:
10-99371069-T-C
gnomAD v3:
10-97611312-T-C
gnomAD v4:
10-97611312-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.97611312T>C , CM000672.2:g.97611312T>C | GRCh38 |
| NC_000010.10:g.99371069T>C , CM000672.1:g.99371069T>C | GRCh37 |
| NC_000010.9:g.99361059T>C | NCBI36 |
| NG_027922.1:g.31968T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370646.9:c.835-198T>C MANE Select | ENSP00000359680.4:n.835-198T>C | |
| ENST00000370646.8:c.835-198T>C | ENSP00000359680.4:n.835-198T>C | |
| ENST00000370647.8:c.346-198T>C | ENSP00000359681.4:n.346-198T>C | |
| ENST00000370649.3:c.345+9322T>C | ENSP00000359683.3:n.345+9322T>C | |
| NM_001134670.1:c.346-198T>C | NP_001128142.1:n.346-198T>C | |
| NM_138413.3:c.835-198T>C | NP_612422.2:n.835-198T>C | |
| NM_138413.4:c.835-198T>C MANE Select | NP_612422.2:n.835-198T>C | |
| NM_001134670.2:c.346-198T>C | NP_001128142.1:n.346-198T>C |