Linked Data
dbSNP Id:
rs1056348246
gnomAD v2:
10-96701479-T-C
gnomAD v3:
10-94941722-T-C
gnomAD v4:
10-94941722-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94941722T>C , CM000672.2:g.94941722T>C | GRCh38 |
| NC_000010.10:g.96701479T>C , CM000672.1:g.96701479T>C | GRCh37 |
| NC_000010.9:g.96691469T>C | NCBI36 |
| NG_008385.1:g.8065T>C | |
| NG_008385.2:g.8565T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260682.8:c.169-136T>C MANE Select | ENSP00000260682.6:n.169-136T>C | |
| ENST00000643112.1:c.169-136T>C | ENSP00000496202.1:n.169-136T>C | |
| ENST00000645207.1:n.186T>C | ||
| ENST00000260682.6:c.169-136T>C | ENSP00000260682.6:n.169-136T>C | |
| ENST00000461906.1:n.194-136T>C | ||
| NM_000771.3:c.169-136T>C | NP_000762.2:n.169-136T>C | |
| NM_000771.4:c.169-136T>C MANE Select | NP_000762.2:n.169-136T>C |