Linked Data
gnomAD v4:
1-94021642-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94021642T>C , CM000663.2:g.94021642T>C | GRCh38 |
| NC_000001.10:g.94487198T>C , CM000663.1:g.94487198T>C | GRCh37 |
| NC_000001.9:g.94259786T>C | NCBI36 |
| NG_009073.1:g.104508A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.4846A>G MANE Select | ENSP00000359245.3:p.Lys1616Glu | |
| ENST00000370225.3:c.4846A>G | ENSP00000359245.3:p.Lys1616Glu | |
| ENST00000460514.1:n.340A>G | ||
| ENST00000536513.5:c.1222A>G | ENSP00000439707.2:p.Lys408Glu | |
| NM_000350.2:c.4846A>G | NP_000341.2:p.Lys1616Glu | |
| NM_000350.3:c.4846A>G MANE Select | NP_000341.2:p.Lys1616Glu |