Linked Data
gnomAD v4:
2-149569762-C-CA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.149569764dup , CM000664.2:g.149569764dup | GRCh38 |
| NC_000002.11:g.150426278dup , CM000664.1:g.150426278dup | GRCh37 |
| NC_000002.10:g.150134524dup | NCBI36 |
| NG_009189.1:g.23054dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303319.10:c.*211dup MANE Select | ENSP00000301920.5:n.*211dup | |
| ENST00000303319.9:c.*211dup | ENSP00000301920.5:n.*211dup | |
| ENST00000422782.2:c.*211dup | ENSP00000408331.2:n.*211dup | |
| ENST00000428879.5:c.*211dup | ENSP00000389060.1:n.*211dup | |
| NM_015702.2:c.*211dup | NP_056517.1:n.*211dup | |
| NM_015702.3:c.*211dup MANE Select | NP_056517.1:n.*211dup |