Linked Data
dbSNP Id:
rs1970457964
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.12887083A>C , CM000681.2:g.12887083A>C | GRCh38 |
| NC_000019.9:g.12997897A>C , CM000681.1:g.12997897A>C | GRCh37 |
| NC_000019.8:g.12858897A>C | NCBI36 |
| NG_009292.1:g.924A>C | |
| NG_013087.1:g.5121T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264834.6:c.58T>G MANE Select | ENSP00000264834.3:p.Phe20Val | |
| ENST00000264834.4:c.58T>G | ENSP00000264834.3:p.Phe20Val | |
| NM_006563.3:c.58T>G | NP_006554.1:p.Phe20Val | |
| XM_011527642.1:c.-146T>G | XP_011525944.1:n.-146T>G | |
| NM_006563.4:c.58T>G | NP_006554.1:p.Phe20Val | |
| XM_011527642.2:c.-146T>G | XP_011525944.1:n.-146T>G | |
| NM_006563.5:c.58T>G MANE Select | NP_006554.1:p.Phe20Val |