Linked Data
dbSNP Id:
rs2099302998
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186079222G>C , CM000666.2:g.186079222G>C | GRCh38 |
| NC_000004.11:g.187000376G>C , CM000666.1:g.187000376G>C | GRCh37 |
| NC_000004.10:g.187237370G>C | NCBI36 |
| NG_007278.1:g.15068G>C , LRG_117:g.15068G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000698351.1:c.633+191G>C | ENSP00000513674.1:n.633+191G>C | |
| ENST00000698352.1:c.*185+191G>C | ENSP00000513675.1:n.*185+191G>C | |
| ENST00000296795.8:c.633+191G>C MANE Select | ENSP00000296795.3:n.633+191G>C | |
| ENST00000296795.7:c.633+191G>C | ENSP00000296795.2:n.633+191G>C | |
| ENST00000513189.1:c.633+191G>C | ENSP00000423386.1:n.633+191G>C | |
| NM_003265.2:c.633+191G>C , LRG_117t1:c.633+191G>C | NP_003256.1:n.633+191G>C | |
| NM_003265.3:c.633+191G>C MANE Select | NP_003256.1:n.633+191G>C |