Linked Data
ClinVar Variation Id:
2989175
ClinVar RCV Id:
RCV003849326
dbSNP Id:
rs528900765
gnomAD v2:
6-64694515-C-A
gnomAD v4:
6-63984622-C-A
MyVariant Identifiers:
chr6:g.64694515_64694516delinsAA (hg19)
chr6:g.63984622_63984623delinsAA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.63984622C>A , CM000668.2:g.63984622C>A | GRCh38 |
| NC_000006.11:g.64694515C>A , CM000668.1:g.64694515C>A | GRCh37 |
| NC_000006.10:g.64752474C>A | NCBI36 |
| NG_023443.1:g.1727604G>T | |
| NG_023443.2:g.1727604G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000503581.6:c.6835-19G>T MANE Select | ENSP00000424243.1:n.6835-19G>T | |
| ENST00000370616.6:c.6835-19G>T | ENSP00000359650.2:n.6835-19G>T | |
| ENST00000370618.7:c.6835-19G>T | ENSP00000359652.4:n.6835-19G>T | |
| ENST00000370621.7:c.6835-19G>T | ENSP00000359655.3:n.6835-19G>T | |
| ENST00000398580.3:c.149-19G>T | ||
| ENST00000503581.5:c.6835-19G>T | ENSP00000424243.1:n.6835-19G>T | |
| NM_001142800.1:c.6835-19G>T | NP_001136272.1:n.6835-19G>T | |
| NM_001292009.1:c.6835-19G>T | NP_001278938.1:n.6835-19G>T | |
| XR_001744188.1:n.606+16338C>A | ||
| XR_001744189.1:n.129+16338C>A | ||
| XR_001744190.1:n.197+16338C>A | ||
| XR_001744191.1:n.607-1032C>A | ||
| NM_001142800.2:c.6835-19G>T MANE Select | NP_001136272.1:n.6835-19G>T | |
| NM_001292009.2:c.6835-19G>T | NP_001278938.1:n.6835-19G>T |