Linked Data
gnomAD v4:
6-32443779-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32443779C>A , CM000668.2:g.32443779C>A | GRCh38 |
| NC_000006.11:g.32411556C>A , CM000668.1:g.32411556C>A | GRCh37 |
| NC_000006.10:g.32519534C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000395388.7:c.634C>A MANE Select | ENSP00000378786.2:p.Pro212Thr | |
| ENST00000374982.5:c.559C>A | ENSP00000364121.5:p.Pro187Thr | |
| ENST00000395388.6:c.634C>A | ENSP00000378786.2:p.Pro212Thr | |
| NM_019111.4:c.634C>A | NP_061984.2:p.Pro212Thr | |
| NM_019111.5:c.634C>A MANE Select | NP_061984.2:p.Pro212Thr |