Linked Data
dbSNP Id:
rs1244667518
gnomAD v2:
4-69536090-T-C
gnomAD v3:
4-68670372-T-C
gnomAD v4:
4-68670372-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.68670372T>C , CM000666.2:g.68670372T>C | GRCh38 |
| NC_000004.11:g.69536090T>C , CM000666.1:g.69536090T>C | GRCh37 |
| NC_000004.10:g.69218685T>C | NCBI36 |
| NG_052676.1:g.5405A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000338206.6:c.247A>G MANE Select | ENSP00000341045.5:p.Lys83Glu | |
| ENST00000338206.5:c.247A>G | ENSP00000341045.5:p.Lys83Glu | |
| ENST00000616841.4:c.247A>G | ENSP00000482004.1:p.Lys83Glu | |
| NM_001076.3:c.247A>G | NP_001067.2:p.Lys83Glu | |
| NM_001076.4:c.247A>G MANE Select | NP_001067.2:p.Lys83Glu |