Linked Data
dbSNP Id:
rs1769306766
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.113387852G>T , CM000667.2:g.113387852G>T | GRCh38 |
| NC_000005.9:g.112723549G>T , CM000667.1:g.112723549G>T | GRCh37 |
| NC_000005.8:g.112751448G>T | NCBI36 |
| NG_012265.1:g.105979C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000408903.7:c.171-2640C>A MANE Select | ENSP00000386227.3:n.171-2640C>A | |
| ENST00000408903.6:c.171-2640C>A | ENSP00000386227.3:n.171-2640C>A | |
| NM_001085377.1:c.171-2640C>A | NP_001078846.1:n.171-2640C>A | |
| XM_017009473.1:c.171-2640C>A | XP_016864962.1:n.171-2640C>A | |
| NM_001085377.2:c.171-2640C>A MANE Select | NP_001078846.2:n.171-2640C>A |