Linked Data
gnomAD v4:
20-10658644-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10658644T>G , CM000682.2:g.10658644T>G | GRCh38 |
| NC_000020.10:g.10639292T>G , CM000682.1:g.10639292T>G | GRCh37 |
| NC_000020.9:g.10587292T>G | NCBI36 |
| NG_007496.1:g.20403A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254958.10:c.518A>C MANE Select | ENSP00000254958.4:p.Asn173Thr | |
| ENST00000254958.9:c.518A>C | ENSP00000254958.4:p.Asn173Thr | |
| ENST00000423891.6:n.384A>C | ||
| NM_000214.2:c.518A>C | NP_000205.1:p.Asn173Thr | |
| NM_000214.3:c.518A>C MANE Select | NP_000205.1:p.Asn173Thr |