Linked Data
dbSNP Id:
rs113853162
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186191703A>T , CM000666.2:g.186191703A>T | GRCh38 |
| NC_000004.11:g.187112857A>T , CM000666.1:g.187112857A>T | GRCh37 |
| NC_000004.10:g.187349851A>T | NCBI36 |
| NG_007965.1:g.5184A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378802.5:c.-121A>T MANE Select | ENSP00000368079.4:n.-121A>T | |
| ENST00000378802.4:c.-121A>T | ENSP00000368079.4:n.-121A>T | |
| NM_207352.3:c.-121A>T | NP_997235.3:n.-121A>T | |
| XM_005262935.2:c.-121A>T | XP_005262992.1:n.-121A>T | |
| XM_017008037.1:c.-431A>T | XP_016863526.1:n.-431A>T | |
| NM_207352.4:c.-121A>T MANE Select | NP_997235.3:n.-121A>T |