Linked Data
dbSNP Id:
rs1695440368
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.191014658G>C , CM000664.2:g.191014658G>C | GRCh38 |
| NC_000002.11:g.191879384G>C , CM000664.1:g.191879384G>C | GRCh37 |
| NC_000002.10:g.191587629G>C | NCBI36 |
| NG_008294.1:g.4593C>G , LRG_111:g.4593C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000432058.1:c.-155-980C>G | ENSP00000416019.1:n.-155-980C>G | |
| ENST00000454414.5:c.-1-4654C>G | ENSP00000411398.1:n.-1-4654C>G |