Linked Data
dbSNP Id:
rs754204938
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1213507C>T , CM000667.2:g.1213507C>T | GRCh38 |
| NC_000005.9:g.1213622C>T , CM000667.1:g.1213622C>T | GRCh37 |
| NC_000005.8:g.1266622C>T | NCBI36 |
| NG_008282.1:g.16913C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000304460.11:c.708C>T MANE Select | ENSP00000305302.10:p.Ile236= | |
| ENST00000304460.10:c.708C>T | ENSP00000305302.10:p.Ile236= | |
| ENST00000515652.5:c.616C>T | ENSP00000425701.1:p.Leu206Phe | |
| NM_001003841.2:c.708C>T | NP_001003841.1:p.Ile236= | |
| NM_001003841.3:c.708C>T MANE Select | NP_001003841.1:p.Ile236= |