Linked Data
gnomAD v4:
2-149569925-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.149569925A>C , CM000664.2:g.149569925A>C | GRCh38 |
| NC_000002.11:g.150426439A>C , CM000664.1:g.150426439A>C | GRCh37 |
| NC_000002.10:g.150134685A>C | NCBI36 |
| NG_009189.1:g.22892T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303319.10:c.*49T>G MANE Select | ENSP00000301920.5:n.*49T>G | |
| ENST00000303319.9:c.*49T>G | ENSP00000301920.5:n.*49T>G | |
| ENST00000422782.2:c.*49T>G | ENSP00000408331.2:n.*49T>G | |
| ENST00000428879.5:c.*49T>G | ENSP00000389060.1:n.*49T>G | |
| NM_015702.2:c.*49T>G | NP_056517.1:n.*49T>G | |
| NM_015702.3:c.*49T>G MANE Select | NP_056517.1:n.*49T>G |