Linked Data
dbSNP Id:
rs902933455
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.159316037T>C , CM000667.2:g.159316037T>C | GRCh38 |
| NC_000005.9:g.158743045T>C , CM000667.1:g.158743045T>C | GRCh37 |
| NC_000005.8:g.158675623T>C | NCBI36 |
| NG_009618.1:g.19437A>G , LRG_71:g.19437A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000696750.1:c.*64A>G | ENSP00000512849.1:n.*64A>G | |
| ENST00000696751.1:c.*546A>G | ENSP00000512850.1:n.*546A>G | |
| ENST00000231228.3:c.*64A>G MANE Select | ENSP00000231228.2:n.*64A>G | |
| ENST00000231228.2:c.*64A>G | ENSP00000231228.2:n.*64A>G | |
| NM_002187.2:c.*64A>G , LRG_71t1:c.*64A>G | NP_002178.2:n.*64A>G | |
| NM_002187.3:c.*64A>G MANE Select | NP_002178.2:n.*64A>G |