Linked Data
dbSNP Id:
rs1214076145
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.89179651C>T , CM000678.2:g.89179651C>T | GRCh38 |
| NC_000016.9:g.89246059C>T , CM000678.1:g.89246059C>T | GRCh37 |
| NC_000016.8:g.87773560C>T | NCBI36 |
| NG_012055.1:g.12897C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000289746.3:c.201+77C>T MANE Select | ENSP00000289746.2:n.201+77C>T | |
| ENST00000289746.2:c.201+77C>T | ENSP00000289746.2:n.201+77C>T | |
| ENST00000521087.5:n.266+77C>T | ||
| ENST00000524089.1:n.266+77C>T | ||
| NM_004933.2:c.201+77C>T | NP_004924.1:n.201+77C>T | |
| XM_011522806.1:c.201+77C>T | XP_011521108.1:n.201+77C>T | |
| NM_004933.3:c.201+77C>T MANE Select | NP_004924.1:n.201+77C>T |