Linked Data
dbSNP Id:
rs1687797889
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.202520248T>G , CM000664.2:g.202520248T>G | GRCh38 |
| NC_000002.11:g.203384971T>G , CM000664.1:g.203384971T>G | GRCh37 |
| NC_000002.10:g.203093216T>G | NCBI36 |
| NG_009363.1:g.148922T>G , LRG_712:g.148922T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374580.10:c.967+47T>G MANE Select | ENSP00000363708.4:n.967+47T>G | |
| ENST00000638587.1:c.898+47T>G | ENSP00000491062.1:n.898+47T>G | |
| ENST00000374574.2:c.967+47T>G | ENSP00000363702.2:n.967+47T>G | |
| ENST00000374580.8:c.967+47T>G | ENSP00000363708.4:n.967+47T>G | |
| NM_001204.6:c.967+47T>G , LRG_712t1:c.967+47T>G | NP_001195.2:n.967+47T>G | |
| XM_011511687.1:c.967+47T>G | XP_011509989.1:n.967+47T>G | |
| XM_011511688.1:c.967+47T>G | XP_011509990.1:n.967+47T>G | |
| NM_001204.7:c.967+47T>G MANE Select | NP_001195.2:n.967+47T>G |