Linked Data
gnomAD v4:
1-171652650-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171652650T>C , CM000663.2:g.171652650T>C | GRCh38 |
| NC_000001.10:g.171621790T>C , CM000663.1:g.171621790T>C | GRCh37 |
| NC_000001.9:g.169888413T>C | NCBI36 |
| NG_008859.1:g.4984A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000037502.11:c.-39A>G MANE Select | ENSP00000037502.5:n.-39A>G | |
| ENST00000037502.10:c.-39A>G | ENSP00000037502.5:n.-39A>G | |
| NM_000261.2:c.-39A>G MANE Select | NP_000252.1:n.-39A>G |