Linked Data
gnomAD v4:
17-74917471-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.74917471C>G , CM000679.2:g.74917471C>G | GRCh38 |
| NC_000017.10:g.72913565C>G , CM000679.1:g.72913565C>G | GRCh37 |
| NC_000017.9:g.70425160C>G | NCBI36 |
| NG_007882.1:g.10787G>C | |
| NG_007882.2:g.10793G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000614341.5:c.*602G>C MANE Select | ENSP00000480279.1:n.*602G>C | |
| ENST00000614341.4:c.*602G>C | ENSP00000480279.1:n.*602G>C | |
| NM_001282489.2:c.*602G>C | NP_001269418.1:n.*602G>C | |
| NM_173477.4:c.*602G>C | NP_775748.2:n.*602G>C | |
| XM_011524296.1:c.*602G>C | XP_011522598.1:n.*602G>C | |
| XM_011524296.2:c.*602G>C | XP_011522598.1:n.*602G>C | |
| NM_173477.5:c.*602G>C MANE Select | NP_775748.2:n.*602G>C | |
| NM_001282489.3:c.*602G>C | NP_001269418.1:n.*602G>C |