Linked Data
dbSNP Id:
rs1456461164
gnomAD v2:
14-101349427-T-C
gnomAD v3:
14-100883090-T-C
gnomAD v4:
14-100883090-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.100883090T>C , CM000676.2:g.100883090T>C | GRCh38 |
| NC_000014.8:g.101349427T>C , CM000676.1:g.101349427T>C | GRCh37 |
| NC_000014.7:g.100419180T>C | NCBI36 |
| NG_045001.1:g.6758A>G | |
| NG_045000.5:g.51822T>C | |
| NG_045000.6:g.51822T>C | |
| NG_045001.2:g.25633A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649591.1:c.1699A>G MANE Select | ENSP00000497482.1:p.Asn567Asp | |
| ENST00000534062.1:c.1699A>G | ENSP00000435342.1:p.Asn567Asp | |
| NM_001134888.2:c.1699A>G | NP_001128360.1:p.Asn567Asp | |
| NM_001134888.3:c.1699A>G MANE Select | NP_001128360.1:p.Asn567Asp |