Linked Data
gnomAD v4:
4-186191653-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186191653T>G , CM000666.2:g.186191653T>G | GRCh38 |
| NC_000004.11:g.187112807T>G , CM000666.1:g.187112807T>G | GRCh37 |
| NC_000004.10:g.187349801T>G | NCBI36 |
| NG_007965.1:g.5134T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378802.5:c.-171T>G MANE Select | ENSP00000368079.4:n.-171T>G | |
| ENST00000378802.4:c.-171T>G | ENSP00000368079.4:n.-171T>G | |
| NM_207352.3:c.-171T>G | NP_997235.3:n.-171T>G | |
| XM_005262935.2:c.-171T>G | XP_005262992.1:n.-171T>G | |
| NM_207352.4:c.-171T>G MANE Select | NP_997235.3:n.-171T>G |