Linked Data
gnomAD v4:
10-94941824-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94941824C>T , CM000672.2:g.94941824C>T | GRCh38 |
| NC_000010.10:g.96701581C>T , CM000672.1:g.96701581C>T | GRCh37 |
| NC_000010.9:g.96691571C>T | NCBI36 |
| NG_008385.1:g.8167C>T | |
| NG_008385.2:g.8667C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260682.8:c.169-34C>T MANE Select | ENSP00000260682.6:n.169-34C>T | |
| ENST00000643112.1:c.169-34C>T | ENSP00000496202.1:n.169-34C>T | |
| ENST00000645207.1:n.288C>T | ||
| ENST00000260682.6:c.169-34C>T | ENSP00000260682.6:n.169-34C>T | |
| ENST00000461906.1:n.194-34C>T | ||
| NM_000771.3:c.169-34C>T | NP_000762.2:n.169-34C>T | |
| NM_000771.4:c.169-34C>T MANE Select | NP_000762.2:n.169-34C>T |