Linked Data
gnomAD v4:
6-143485171-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.143485171C>T , CM000668.2:g.143485171C>T | GRCh38 |
| NC_000006.11:g.143806308C>T , CM000668.1:g.143806308C>T | GRCh37 |
| NC_000006.10:g.143848001C>T | NCBI36 |
| NG_008459.1:g.39391C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367591.5:c.961C>T MANE Select | ENSP00000356563.4:p.Pro321Ser | |
| ENST00000367591.4:c.961C>T | ENSP00000356563.4:p.Pro321Ser | |
| ENST00000585848.1:n.100C>T | ||
| NM_003630.2:c.961C>T | NP_003621.1:p.Pro321Ser | |
| NM_003630.3:c.961C>T MANE Select | NP_003621.1:p.Pro321Ser |