Linked Data
dbSNP Id:
rs1694925169
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.208124084C>G , CM000664.2:g.208124084C>G | GRCh38 |
| NC_000002.11:g.208988808C>G , CM000664.1:g.208988808C>G | GRCh37 |
| NC_000002.10:g.208697053C>G | NCBI36 |
| NG_008039.1:g.5506G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264376.5:c.252+28G>C MANE Select | ENSP00000264376.4:n.252+28G>C | |
| ENST00000264376.4:c.252+28G>C | ENSP00000264376.4:n.252+28G>C | |
| NM_006891.3:c.252+28G>C | NP_008822.2:n.252+28G>C | |
| NR_038437.1:n.97+4859C>G | ||
| NM_006891.4:c.252+28G>C MANE Select | NP_008822.2:n.252+28G>C |