Linked Data
dbSNP Id:
rs1227813049
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.212883357A>C , CM000663.2:g.212883357A>C | GRCh38 |
| NC_000001.10:g.213056699A>C , CM000663.1:g.213056699A>C | GRCh37 |
| NC_000001.9:g.211123322A>C | NCBI36 |
| NG_028131.1:g.30103A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000366971.9:c.1025-14A>C MANE Select | ENSP00000355938.4:n.1025-14A>C | |
| ENST00000366971.8:c.1025-14A>C | ENSP00000355938.4:n.1025-14A>C | |
| ENST00000419102.1:c.421-14A>C | ||
| ENST00000474693.1:n.250-14A>C | ||
| NM_014053.3:c.1025-14A>C | NP_054772.1:n.1025-14A>C | |
| XM_011509446.1:c.1025-14A>C | XP_011507748.1:n.1025-14A>C | |
| XR_247024.1:n.1199-14A>C | ||
| XR_426771.1:n.1326-14A>C | ||
| XM_011509446.3:c.1025-14A>C | XP_011507748.1:n.1025-14A>C | |
| XR_247024.3:n.1199-14A>C | ||
| NM_014053.4:c.1025-14A>C MANE Select | NP_054772.1:n.1025-14A>C |