Linked Data
dbSNP Id:
rs1359146648
gnomAD v2:
8-19815205-T-C
gnomAD v3:
8-19957694-T-C
gnomAD v4:
8-19957694-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19957694T>C , CM000670.2:g.19957694T>C | GRCh38 |
| NC_000008.10:g.19815205T>C , CM000670.1:g.19815205T>C | GRCh37 |
| NC_000008.9:g.19859485T>C | NCBI36 |
| NG_008855.1:g.23624T>C | |
| NG_008855.2:g.60978T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000650287.1:c.1019-1566T>C MANE Select | ENSP00000497642.1:n.1019-1566T>C | |
| ENST00000650478.1:c.79+1611T>C | ENSP00000497560.1:n.79+1611T>C | |
| ENST00000311322.8:c.1019-1566T>C | ENSP00000309757.6:n.1019-1566T>C | |
| NM_000237.2:c.1019-1566T>C | NP_000228.1:n.1019-1566T>C | |
| NM_000237.3:c.1019-1566T>C MANE Select | NP_000228.1:n.1019-1566T>C |