Linked Data
ClinVar Variation Id:
1686781
ClinVar RCV Id:
RCV002248286
dbSNP Id:
rs143413116
ExAC:
1:171621481 G / A
gnomAD v2:
1-171621481-G-A
gnomAD v4:
1-171652341-G-A
ERepo:
CA1244303/MONDO:0020367/019
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171652341G>A , CM000663.2:g.171652341G>A | GRCh38 |
| NC_000001.10:g.171621481G>A , CM000663.1:g.171621481G>A | GRCh37 |
| NC_000001.9:g.169888104G>A | NCBI36 |
| NG_008859.1:g.5293C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000037502.11:c.271C>T MANE Select | ENSP00000037502.5:p.Arg91Ter | |
| ENST00000638471.1:c.130+141C>T | ENSP00000491206.1:n.130+141C>T | |
| ENST00000037502.10:c.271C>T | ENSP00000037502.5:p.Arg91Ter | |
| ENST00000614688.1:c.271C>T | ENSP00000478680.1:p.Arg91Ter | |
| NM_000261.1:c.271C>T | NP_000252.1:p.Arg91Ter | |
| NM_000261.2:c.271C>T MANE Select | NP_000252.1:p.Arg91Ter |