Linked Data
dbSNP Id:
rs1268967349
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154896231A>C , CM000685.2:g.154896231A>C | GRCh38 |
| NC_000023.10:g.154124506A>C , CM000685.1:g.154124506A>C | GRCh37 |
| NC_000023.9:g.153777700A>C | NCBI36 |
| NG_011403.1:g.131493T>G | |
| NG_011403.2:g.131493T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000360256.9:c.6275T>G MANE Select | ENSP00000353393.4:p.Val2092Gly | |
| ENST00000360256.8:c.6275T>G | ENSP00000353393.4:p.Val2092Gly | |
| NM_000132.3:c.6275T>G | NP_000123.1:p.Val2092Gly | |
| XM_011531126.1:c.6170T>G | XP_011529428.1:p.Val2057Gly | |
| NM_000132.4:c.6275T>G MANE Select | NP_000123.1:p.Val2092Gly |