Linked Data
ClinVar Variation Id:
329357
dbSNP Id:
rs140322984
ExAC:
19:41903795 C / T
gnomAD v2:
19-41903795-C-T
gnomAD v3:
19-41397890-C-T
gnomAD v4:
19-41397890-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.41397890C>T , CM000681.2:g.41397890C>T | GRCh38 |
| NC_000019.9:g.41903795C>T , CM000681.1:g.41903795C>T | GRCh37 |
| NC_000019.8:g.46595635C>T | NCBI36 |
| NG_013004.1:g.5102C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000269980.7:c.63C>T MANE Select | ENSP00000269980.2:p.Ala21= | |
| ENST00000269980.6:c.63C>T | ENSP00000269980.2:p.Ala21= | |
| ENST00000457836.6:c.57+6C>T | ENSP00000416000.2:n.57+6C>T | |
| ENST00000538423.5:n.83C>T | ||
| ENST00000540732.3:c.211-12747C>T | ENSP00000443246.1:n.211-12747C>T | |
| ENST00000542943.5:c.63C>T | ENSP00000440345.1:p.Ala21= | |
| ENST00000595085.5:c.63C>T | ENSP00000471150.2:p.Ala21= | |
| ENST00000604424.1:n.351-12747C>T | ||
| NM_000709.3:c.63C>T | NP_000700.1:p.Ala21= | |
| NM_001164783.1:c.63C>T | NP_001158255.1:p.Ala21= | |
| NM_000709.4:c.63C>T MANE Select | NP_000700.1:p.Ala21= | |
| NM_001164783.2:c.63C>T | NP_001158255.1:p.Ala21= |