Linked Data
ClinVar Variation Id:
2170836
ClinVar RCV Id:
RCV003080743
dbSNP Id:
rs948621105
gnomAD v4:
9-2115944-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.2115944C>T , CM000671.2:g.2115944C>T | GRCh38 |
| NC_000009.11:g.2115944C>T , CM000671.1:g.2115944C>T | GRCh37 |
| NC_000009.10:g.2105944C>T | NCBI36 |
| NG_032162.1:g.105603C>T | |
| NG_032162.2:g.140655C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000704350.1:c.3219C>T | ENSP00000515861.1:p.Asn1073= | |
| ENST00000704352.1:c.1174-45742C>T | ENSP00000515863.1:n.1174-45742C>T | |
| ENST00000704353.1:c.1174-45742C>T | ENSP00000515864.1:n.1174-45742C>T | |
| ENST00000704354.1:c.3563C>T | ||
| ENST00000704355.1:c.1943C>T | ||
| ENST00000349721.8:c.3579C>T MANE Select | ENSP00000265773.5:p.Asn1193= | |
| ENST00000357248.8:c.3579C>T | ENSP00000349788.2:p.Asn1193= | |
| ENST00000635739.1:n.2247C>T | ||
| ENST00000636157.1:n.1186C>T | ||
| ENST00000638139.1:n.613C>T | ||
| ENST00000349721.7:c.3579C>T | ENSP00000265773.5:p.Asn1193= | |
| ENST00000357248.7:c.3579C>T | ENSP00000349788.2:p.Asn1193= | |
| ENST00000382194.6:c.3579C>T | ENSP00000371629.1:p.Asn1193= | |
| ENST00000382203.5:c.3579C>T | ENSP00000371638.1:p.Asn1193= | |
| ENST00000450198.6:c.3405C>T | ENSP00000392081.2:p.Asn1135= | |
| ENST00000634760.1:c.3579C>T | ENSP00000489256.1:p.Asn1193= | |
| ENST00000634772.1:c.62-3514C>T | ||
| ENST00000634925.1:n.1070C>T | ||
| NM_001289396.1:c.3579C>T | NP_001276325.1:p.Asn1193= | |
| NM_001289397.1:c.3405C>T | NP_001276326.1:p.Asn1135= | |
| NM_003070.4:c.3579C>T | NP_003061.3:p.Asn1193= | |
| NM_139045.3:c.3579C>T | NP_620614.2:p.Asn1193= | |
| NM_003070.5:c.3579C>T MANE Select | NP_003061.3:p.Asn1193= | |
| NM_001289397.2:c.3405C>T | NP_001276326.1:p.Asn1135= | |
| NM_139045.4:c.3579C>T | NP_620614.2:p.Asn1193= |