Linked Data
dbSNP Id:
rs1165919252
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133261597C>G , CM000671.2:g.133261597C>G | GRCh38 |
| NC_000009.11:g.136137000C>G , CM000671.1:g.136137000C>G | GRCh37 |
| NC_000009.10:g.135126821C>G | NCBI36 |
| NG_006669.1:g.16053G>C | |
| NG_006669.2:g.18618G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000453660.4:n.129-223G>C | ||
| ENST00000647353.1:n.54-10445G>C | ||
| ENST00000651471.1:n.134-223G>C | ||
| ENST00000679909.1:c.28+13565G>C | ENSP00000506089.1:n.28+13565G>C | |
| ENST00000453660.3:n.111-223G>C | ||
| ENST00000538324.2:c.99-223G>C | ENSP00000483018.1:n.99-223G>C | |
| ENST00000611156.4:c.99-223G>C | ENSP00000483265.1:n.99-223G>C | |
| NM_020469.2:c.99-223G>C | NP_065202.2:n.99-223G>C | |
| NM_020469.3:c.99-223G>C | NP_065202.2:n.99-223G>C |