Linked Data
dbSNP Id:
rs953316255
gnomAD v4:
11-5233900-C-G
MyVariant Identifiers:
chr11:g.5233900C>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5233900C>G , CM000673.2:g.5233900C>G | GRCh38 |
| NC_000011.9:g.5255130C>G , CM000673.1:g.5255130C>G | GRCh37 |
| NC_000011.8:g.5211706C>G | NCBI36 |
| NG_000007.3:g.63716G>C | |
| NG_063112.2:g.14758G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000643122.1:c.315+91G>C | ENSP00000494708.1:n.315+91G>C | |
| ENST00000650601.1:c.315+91G>C MANE Select | ENSP00000497529.1:n.315+91G>C | |
| ENST00000292901.7:c.315+91G>C | ENSP00000292901.3:n.315+91G>C | |
| ENST00000380299.3:c.315+91G>C | ENSP00000369654.3:n.315+91G>C | |
| ENST00000417377.1:c.92+442G>C | ENSP00000414741.1:n.92+442G>C | |
| NM_000519.3:c.315+91G>C | NP_000510.1:n.315+91G>C | |
| NM_000519.4:c.315+91G>C MANE Select | NP_000510.1:n.315+91G>C |