Linked Data
gnomAD v4:
6-31139489-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31139489C>T , CM000668.2:g.31139489C>T | GRCh38 |
| NC_000006.11:g.31107266C>T , CM000668.1:g.31107266C>T | GRCh37 |
| NC_000006.10:g.31215245C>T | NCBI36 |
| NG_021348.1:g.29659C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259881.10:c.168-152C>T MANE Select | ENSP00000259881.9:n.168-152C>T | |
| ENST00000259881.9:c.168-152C>T | ENSP00000259881.9:n.168-152C>T | |
| ENST00000479581.5:n.62-152C>T | ||
| ENST00000481450.2:c.-22-152C>T | ENSP00000447158.1:n.-22-152C>T | |
| ENST00000547221.1:c.24-152C>T | ENSP00000449471.1:n.24-152C>T | |
| NM_014068.2:c.168-152C>T | NP_054787.2:n.168-152C>T | |
| NM_014068.3:c.168-152C>T MANE Select | NP_054787.2:n.168-152C>T |