Linked Data
dbSNP Id:
rs1838569178
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.62518958C>T , CM000672.2:g.62518958C>T | GRCh38 |
| NC_000010.10:g.64278717C>T , CM000672.1:g.64278717C>T | GRCh37 |
| NC_000010.9:g.63948723C>T | NCBI36 |
| NG_021209.1:g.149802C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647733.1:c.981+59161C>T | ENSP00000502188.1:n.981+59161C>T | |
| ENST00000410046.7:c.981+59161C>T | ENSP00000387091.3:n.981+59161C>T | |
| NM_199451.2:c.981+59161C>T | NP_955523.1:n.981+59161C>T | |
| XM_017015937.2:c.982-25251C>T | XP_016871426.1:n.982-25251C>T | |
| NM_199451.3:c.981+59161C>T | NP_955523.1:n.981+59161C>T |