Linked Data
dbSNP Id:
rs965313701
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63959169G>C , CM000679.2:g.63959169G>C | GRCh38 |
| NC_000017.10:g.62036529G>C , CM000679.1:g.62036529G>C | GRCh37 |
| NC_000017.9:g.59390261G>C | NCBI36 |
| NG_011699.1:g.18750C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000435607.3:c.2019+96C>G MANE Select | ENSP00000396320.1:n.2019+96C>G | |
| ENST00000578147.5:c.2019+96C>G | ENSP00000463963.1:n.2019+96C>G | |
| NM_000334.4:c.2019+96C>G MANE Select | NP_000325.4:n.2019+96C>G | |
| XM_005257566.3:c.2019+96C>G | XP_005257623.1:n.2019+96C>G |