Linked Data
dbSNP Id:
rs1599156221
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.2274795A>C , CM000681.2:g.2274795A>C | GRCh38 |
| NC_000019.9:g.2274794A>C , CM000681.1:g.2274794A>C | GRCh37 |
| NC_000019.8:g.2225794A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342063.5:c.*885T>G MANE Select | ENSP00000345102.3:n.*885T>G | |
| ENST00000342063.4:c.*885T>G | ENSP00000345102.3:n.*885T>G | |
| ENST00000621615.1:c.146+5051A>C | ENSP00000481965.1:n.146+5051A>C | |
| NM_198532.2:c.*885T>G | NP_940934.1:n.*885T>G | |
| NM_198532.3:c.*885T>G MANE Select | NP_940934.1:n.*885T>G |