Linked Data
dbSNP Id:
rs410168
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.33005736C>T , CM000668.2:g.33005736C>T | GRCh38 |
| NC_000006.11:g.32973513C>T , CM000668.1:g.32973513C>T | GRCh37 |
| NC_000006.10:g.33081491C>T | NCBI36 |
| NG_012007.1:g.8877G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000229829.7:c.*1102G>A MANE Select | ENSP00000229829.3:n.*1102G>A | |
| ENST00000229829.6:c.*1102G>A | ENSP00000229829.3:n.*1102G>A | |
| NM_002119.3:c.*1102G>A | NP_002110.1:n.*1102G>A | |
| NM_002119.4:c.*1102G>A MANE Select | NP_002110.1:n.*1102G>A |