Linked Data
gnomAD v4:
2-26135088-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.26135088C>T , CM000664.2:g.26135088C>T | GRCh38 |
| NC_000002.11:g.26357957C>T , CM000664.1:g.26357957C>T | GRCh37 |
| NC_000002.10:g.26211461C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264710.5:c.*67C>T MANE Select | ENSP00000264710.4:n.*67C>T | |
| ENST00000264710.4:c.*67C>T | ENSP00000264710.4:n.*67C>T | |
| ENST00000495146.5:n.1033C>T | ||
| NM_016131.4:c.*67C>T | NP_057215.3:n.*67C>T | |
| XM_024452565.1:c.*67C>T | XP_024308333.1:n.*67C>T | |
| NM_016131.5:c.*67C>T MANE Select | NP_057215.3:n.*67C>T |