Linked Data
dbSNP Id:
rs1516797
gnomAD v2:
15-89410314-T-G
gnomAD v3:
15-88867083-T-G
gnomAD v4:
15-88867083-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.88867083T>G , CM000677.2:g.88867083T>G | GRCh38 |
| NC_000015.9:g.89410314T>G , CM000677.1:g.89410314T>G | GRCh37 |
| NC_000015.8:g.87211318T>G | NCBI36 |
| NG_012794.1:g.68641T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000439576.7:c.6947-4299T>G | ENSP00000387356.2:n.6947-4299T>G | |
| ENST00000560601.4:c.6947-1133T>G MANE Select | ENSP00000453581.2:n.6947-1133T>G | |
| ENST00000561243.7:c.6833-1133T>G | ENSP00000453342.3:n.6833-1133T>G | |
| ENST00000352105.11:c.6833-4299T>G | ENSP00000341615.7:n.6833-4299T>G | |
| ENST00000439576.6:c.6947-4299T>G | ENSP00000387356.2:n.6947-4299T>G | |
| ENST00000559004.5:c.6833-4299T>G | ENSP00000453499.1:n.6833-4299T>G | |
| ENST00000560601.1:c.457-1133T>G | ||
| ENST00000561243.5:c.6947-4299T>G | ENSP00000453342.1:n.6947-4299T>G | |
| ENST00000617301.4:c.6776-4299T>G | ENSP00000484456.1:n.6776-4299T>G | |
| NM_001135.3:c.6833-4299T>G | NP_001126.3:n.6833-4299T>G | |
| NM_013227.3:c.6947-4299T>G | NP_037359.3:n.6947-4299T>G | |
| XM_006720419.1:c.6947-1133T>G | XP_006720482.1:n.6947-1133T>G | |
| XM_011521313.1:c.6833-1133T>G | XP_011519615.1:n.6833-1133T>G | |
| XM_011521314.1:c.6833-4299T>G | XP_011519616.1:n.6833-4299T>G | |
| NM_001369268.1:c.6947-1133T>G MANE Select | NP_001356197.1:n.6947-1133T>G | |
| NM_001135.4:c.6833-4299T>G | NP_001126.3:n.6833-4299T>G | |
| NM_013227.4:c.6947-4299T>G | NP_037359.3:n.6947-4299T>G |