Linked Data
dbSNP Id:
rs1046573886
gnomAD v2:
12-1865856-T-G
gnomAD v3:
12-1756690-T-G
gnomAD v4:
12-1756690-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.1756690T>G , CM000674.2:g.1756690T>G | GRCh38 |
| NC_000012.11:g.1865856T>G , CM000674.1:g.1865856T>G | GRCh37 |
| NC_000012.10:g.1736117T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000357103.5:c.171+2176T>G MANE Select | ENSP00000349616.4:n.171+2176T>G | |
| ENST00000357103.4:c.171+2176T>G | ENSP00000349616.4:n.171+2176T>G | |
| ENST00000537545.1:n.401+2176T>G | ||
| NM_024551.2:c.171+2176T>G | NP_078827.2:n.171+2176T>G | |
| XM_005253789.1:c.171+2176T>G | XP_005253846.1:n.171+2176T>G | |
| XM_006719018.1:c.171+2176T>G | XP_006719081.1:n.171+2176T>G | |
| XM_011521024.1:c.171+2176T>G | XP_011519326.1:n.171+2176T>G | |
| XM_011521025.1:c.171+2176T>G | XP_011519327.1:n.171+2176T>G | |
| XM_005253789.2:c.171+2176T>G | XP_005253846.1:n.171+2176T>G | |
| XM_006719018.2:c.171+2176T>G | XP_006719081.1:n.171+2176T>G | |
| XM_011521024.2:c.171+2176T>G | XP_011519326.1:n.171+2176T>G | |
| NM_024551.3:c.171+2176T>G MANE Select | NP_078827.2:n.171+2176T>G | |
| NM_001375363.1:c.171+2176T>G | NP_001362292.1:n.171+2176T>G | |
| NM_001375364.1:c.171+2176T>G | NP_001362293.1:n.171+2176T>G | |
| NM_001375365.1:c.171+2176T>G | NP_001362294.1:n.171+2176T>G |