Linked Data
ClinVar Variation Id:
1633187
ClinVar RCV Id:
RCV002121668
dbSNP Id:
rs2102748053
gnomAD v4:
1-215766672-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215766672T>C , CM000663.2:g.215766672T>C | GRCh38 |
| NC_000001.10:g.215940014T>C , CM000663.1:g.215940014T>C | GRCh37 |
| NC_000001.9:g.214006637T>C | NCBI36 |
| NG_009497.1:g.661725A>G | |
| NG_009497.2:g.661777A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.11047+9A>G MANE Select | ENSP00000305941.3:n.11047+9A>G | |
| ENST00000674083.1:c.11047+9A>G | ENSP00000501296.1:n.11047+9A>G | |
| ENST00000307340.7:c.11047+9A>G | ENSP00000305941.3:n.11047+9A>G | |
| NM_206933.2:c.11047+9A>G | NP_996816.2:n.11047+9A>G | |
| NM_206933.3:c.11047+9A>G | NP_996816.2:n.11047+9A>G | |
| NM_206933.4:c.11047+9A>G MANE Select | NP_996816.3:n.11047+9A>G |