Linked Data
gnomAD v4:
1-119422889-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.119422889G>A , CM000663.2:g.119422889G>A | GRCh38 |
| NC_000001.10:g.119965512G>A , CM000663.1:g.119965512G>A | GRCh37 |
| NC_000001.9:g.119767035G>A | NCBI36 |
| NG_013349.1:g.12959G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369416.4:c.*269G>A MANE Select | ENSP00000358424.3:n.*269G>A | |
| ENST00000369416.3:c.*269G>A | ENSP00000358424.3:n.*269G>A | |
| ENST00000543831.5:c.*269G>A | ENSP00000445122.1:n.*269G>A | |
| NM_000198.3:c.*269G>A | NP_000189.1:n.*269G>A | |
| NM_001166120.1:c.*269G>A | NP_001159592.1:n.*269G>A | |
| NM_000198.4:c.*269G>A MANE Select | NP_000189.1:n.*269G>A | |
| NM_001166120.2:c.*269G>A | NP_001159592.1:n.*269G>A |