Linked Data
dbSNP Id:
rs1691335045
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.232523698T>C , CM000664.2:g.232523698T>C | GRCh38 |
| NC_000002.11:g.233388408T>C , CM000664.1:g.233388408T>C | GRCh37 |
| NC_000002.10:g.233096652T>C | NCBI36 |
| NG_008028.1:g.2487T>C | |
| NG_031969.1:g.8236T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000617714.2:c.1013-74T>C MANE Select | ENSP00000479745.1:n.1013-74T>C | |
| ENST00000449534.6:c.1013-71T>C | ENSP00000473410.1:n.1013-71T>C | |
| ENST00000617714.1:c.1013-74T>C | ENSP00000479745.1:n.1013-74T>C | |
| NM_001195129.1:c.1013-74T>C | NP_001182058.1:n.1013-74T>C | |
| NM_001195129.2:c.1013-74T>C MANE Select | NP_001182058.1:n.1013-74T>C | |
| NM_001369848.1:c.1013-71T>C | NP_001356777.1:n.1013-71T>C |