Linked Data
dbSNP Id:
rs1654948629
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.197039223A>C , CM000663.2:g.197039223A>C | GRCh38 |
| NC_000001.10:g.197008353A>C , CM000663.1:g.197008353A>C | GRCh37 |
| NC_000001.9:g.195274976A>C | NCBI36 |
| NG_012065.1:g.33045T>G , LRG_550:g.33045T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367412.2:c.*155T>G MANE Select | ENSP00000356382.2:n.*155T>G | |
| ENST00000649282.1:c.896T>G | ENSP00000497116.1:n.896T>G | |
| ENST00000367412.1:c.*155T>G | ENSP00000356382.1:n.*155T>G | |
| NM_001994.2:c.*155T>G , LRG_550t1:c.*155T>G | NP_001985.2:n.*155T>G | |
| XM_011509283.2:c.*1076T>G | XP_011507585.1:n.*1076T>G | |
| XM_011509284.2:c.*1076T>G | XP_011507586.1:n.*1076T>G | |
| XM_011509286.2:c.*1076T>G | XP_011507588.1:n.*1076T>G | |
| NM_001994.3:c.*155T>G MANE Select | NP_001985.2:n.*155T>G |