Linked Data
dbSNP Id:
rs549303552
ExAC:
12:6127768 T / C
gnomAD v2:
12-6127768-T-C
gnomAD v3:
12-6018602-T-C
gnomAD v4:
12-6018602-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.6018602T>C , CM000674.2:g.6018602T>C | GRCh38 |
| NC_000012.11:g.6127768T>C , CM000674.1:g.6127768T>C | GRCh37 |
| NC_000012.10:g.5998029T>C | NCBI36 |
| NG_009072.1:g.111069A>G | |
| NG_009072.2:g.111069A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261405.10:c.4816A>G MANE Select | ENSP00000261405.5:p.Met1606Val | |
| ENST00000261405.9:c.4816A>G | ENSP00000261405.5:p.Met1606Val | |
| ENST00000538635.5:n.421-24668A>G | ||
| NM_000552.3:c.4816A>G | NP_000543.2:p.Met1606Val | |
| NM_000552.4:c.4816A>G | NP_000543.2:p.Met1606Val | |
| NM_000552.5:c.4816A>G MANE Select | NP_000543.3:p.Met1606Val |