Linked Data
dbSNP Id:
rs10500856
gnomAD v2:
11-19584502-A-G
gnomAD v3:
11-19562955-A-G
gnomAD v4:
11-19562955-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.19562955A>G , CM000673.2:g.19562955A>G | GRCh38 |
| NC_000011.9:g.19584502A>G , CM000673.1:g.19584502A>G | GRCh37 |
| NC_000011.8:g.19541078A>G | NCBI36 |
| NG_030347.1:g.217232A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000360655.8:c.75+211928A>G | ENSP00000353871.4:n.75+211928A>G | |
| NM_001111018.1:c.75+211928A>G | NP_001104488.1:n.75+211928A>G | |
| XM_011520452.1:c.75+211928A>G | XP_011518754.1:n.75+211928A>G | |
| XM_011520452.2:c.75+211928A>G | XP_011518754.1:n.75+211928A>G | |
| XM_017018520.2:c.75+211928A>G | XP_016874009.1:n.75+211928A>G | |
| XM_017018522.1:c.75+211928A>G | XP_016874011.1:n.75+211928A>G | |
| XM_024448758.1:c.75+211928A>G | XP_024304526.1:n.75+211928A>G | |
| NM_001111018.2:c.75+211928A>G | NP_001104488.1:n.75+211928A>G |