Linked Data
dbSNP Id:
rs372967761
gnomAD v2:
19-41928520-C-T
gnomAD v3:
19-41422615-C-T
gnomAD v4:
19-41422615-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.41422615C>T , CM000681.2:g.41422615C>T | GRCh38 |
| NC_000019.9:g.41928520C>T , CM000681.1:g.41928520C>T | GRCh37 |
| NC_000019.8:g.46620360C>T | NCBI36 |
| NG_013004.1:g.29827C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000269980.7:c.854-14C>T MANE Select | ENSP00000269980.2:n.854-14C>T | |
| ENST00000269980.6:c.854-14C>T | ENSP00000269980.2:n.854-14C>T | |
| ENST00000457836.6:c.788-14C>T | ENSP00000416000.2:n.788-14C>T | |
| ENST00000535632.5:n.483-14C>T | ||
| ENST00000540732.3:c.956-14C>T | ENSP00000443246.1:n.956-14C>T | |
| ENST00000542943.5:c.767-14C>T | ENSP00000440345.1:n.767-14C>T | |
| ENST00000545787.1:n.482-14C>T | ||
| ENST00000595085.5:c.854-14C>T | ENSP00000471150.2:n.854-14C>T | |
| NM_000709.3:c.854-14C>T | NP_000700.1:n.854-14C>T | |
| NM_001164783.1:c.854-17C>T | NP_001158255.1:n.854-17C>T | |
| NM_000709.4:c.854-14C>T MANE Select | NP_000700.1:n.854-14C>T | |
| NM_001164783.2:c.854-17C>T | NP_001158255.1:n.854-17C>T |