Linked Data
dbSNP Id:
rs771875420
ExAC:
19:15990147 C / T
gnomAD v2:
19-15990147-C-T
gnomAD v3:
19-15879337-C-T
gnomAD v4:
19-15879337-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.15879337C>T , CM000681.2:g.15879337C>T | GRCh38 |
| NC_000019.9:g.15990147C>T , CM000681.1:g.15990147C>T | GRCh37 |
| NC_000019.8:g.15851147C>T | NCBI36 |
| NG_007971.2:g.23738G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000221700.11:c.1397+9G>A MANE Select | ENSP00000221700.3:n.1397+9G>A | |
| ENST00000011989.11:c.1397+9G>A | ENSP00000011989.8:n.1397+9G>A | |
| ENST00000221700.10:c.1397+9G>A | ENSP00000221700.3:n.1397+9G>A | |
| ENST00000392846.7:n.1340+9G>A | ||
| ENST00000589654.2:c.185+9G>A | ||
| NM_001082.4:c.1397+9G>A | NP_001073.3:n.1397+9G>A | |
| NM_001082.5:c.1397+9G>A MANE Select | NP_001073.3:n.1397+9G>A |