Linked Data
dbSNP Id:
rs981745597
gnomAD v2:
16-23222888-T-C
gnomAD v3:
16-23211567-T-C
gnomAD v4:
16-23211567-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.23211567T>C , CM000678.2:g.23211567T>C | GRCh38 |
| NC_000016.9:g.23222888T>C , CM000678.1:g.23222888T>C | GRCh37 |
| NC_000016.8:g.23130389T>C | NCBI36 |
| NG_011909.1:g.33849T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000300061.3:c.1177-467T>C MANE Select | ENSP00000300061.2:n.1177-467T>C | |
| ENST00000300061.2:c.1177-467T>C | ENSP00000300061.2:n.1177-467T>C | |
| NM_001039.3:c.1177-467T>C | NP_001030.2:n.1177-467T>C | |
| NM_001039.4:c.1177-467T>C MANE Select | NP_001030.2:n.1177-467T>C |