Linked Data
dbSNP Id:
rs754381626
ExAC:
6:30890544 C / T
gnomAD v2:
6-30890544-C-T
gnomAD v4:
6-30922767-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.30922767C>T , CM000668.2:g.30922767C>T | GRCh38 |
| NC_000006.11:g.30890544C>T , CM000668.1:g.30890544C>T | GRCh37 |
| NC_000006.10:g.30998523C>T | NCBI36 |
| NG_034224.1:g.13560C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000541562.6:c.2099C>T | ENSP00000441000.2:p.Ala700Val | |
| ENST00000672801.1:c.2093C>T | ENSP00000500615.1:p.Ala698Val | |
| ENST00000676266.1:c.2099C>T MANE Select | ENSP00000502585.1:p.Ala700Val | |
| ENST00000321897.9:c.2099C>T | ENSP00000316092.5:p.Ala700Val | |
| ENST00000469358.5:n.2087C>T | ||
| ENST00000476162.5:n.886C>T | ||
| ENST00000477052.1:n.185C>T | ||
| ENST00000477288.5:n.4712C>T | ||
| ENST00000541562.5:c.2189C>T | ENSP00000441000.1:p.Ala730Val | |
| ENST00000542001.5:c.2093C>T | ENSP00000438200.2:p.Ala698Val | |
| ENST00000625423.2:c.1679C>T | ENSP00000485818.1:p.Ala560Val | |
| NM_001167733.2:c.1679C>T | NP_001161205.1:p.Ala560Val | |
| NM_001167734.1:c.2189C>T | NP_001161206.1:p.Ala730Val | |
| NM_020442.5:c.2099C>T | NP_065175.4:p.Ala700Val | |
| NM_001167733.3:c.1679C>T | NP_001161205.1:p.Ala560Val | |
| NM_001167734.2:c.2189C>T | NP_001161206.1:p.Ala730Val | |
| NM_020442.6:c.2099C>T MANE Select | NP_065175.4:p.Ala700Val |