Linked Data
dbSNP Id:
rs1343585635
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.18393526T>G , CM000670.2:g.18393526T>G | GRCh38 |
| NC_000008.10:g.18251036T>G , CM000670.1:g.18251036T>G | GRCh37 |
| NC_000008.9:g.18295316T>G | NCBI36 |
| NG_012246.1:g.7282T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000286479.4:c.-7+2181T>G MANE Select | ENSP00000286479.3:n.-7+2181T>G | |
| ENST00000286479.3:c.-7+2181T>G | ENSP00000286479.3:n.-7+2181T>G | |
| ENST00000520116.1:c.-58+2181T>G | ENSP00000428416.1:n.-58+2181T>G | |
| NM_000015.2:c.-7+2181T>G | NP_000006.2:n.-7+2181T>G | |
| XM_011544358.1:c.-7+790T>G | XP_011542660.1:n.-7+790T>G | |
| XM_017012938.1:c.-6-6472T>G | XP_016868427.1:n.-6-6472T>G | |
| NM_000015.3:c.-7+2181T>G MANE Select | NP_000006.2:n.-7+2181T>G |