Linked Data
dbSNP Id:
rs747742003
ExAC:
4:69535929 T / C
gnomAD v2:
4-69535929-T-C
gnomAD v3:
4-68670211-T-C
gnomAD v4:
4-68670211-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.68670211T>C , CM000666.2:g.68670211T>C | GRCh38 |
| NC_000004.11:g.69535929T>C , CM000666.1:g.69535929T>C | GRCh37 |
| NC_000004.10:g.69218524T>C | NCBI36 |
| NG_052676.1:g.5566A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000338206.6:c.408A>G MANE Select | ENSP00000341045.5:p.Lys136= | |
| ENST00000338206.5:c.408A>G | ENSP00000341045.5:p.Lys136= | |
| ENST00000616841.4:c.408A>G | ENSP00000482004.1:p.Lys136= | |
| NM_001076.3:c.408A>G | NP_001067.2:p.Lys136= | |
| NM_001076.4:c.408A>G MANE Select | NP_001067.2:p.Lys136= |