Linked Data
dbSNP Id:
rs764587853
ExAC:
14:29237319 C / T
gnomAD v2:
14-29237319-C-T
gnomAD v4:
14-28768113-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.28768113C>T , CM000676.2:g.28768113C>T | GRCh38 |
| NC_000014.8:g.29237319C>T , CM000676.1:g.29237319C>T | GRCh37 |
| NC_000014.7:g.28307070C>T | NCBI36 |
| NG_009367.1:g.6033C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000706482.1:c.834C>T | ENSP00000516406.1:p.Thr278= | |
| ENST00000313071.7:c.834C>T MANE Select | ENSP00000339004.3:p.Thr278= | |
| ENST00000313071.6:c.834C>T | ENSP00000339004.3:p.Thr278= | |
| NM_005249.4:c.834C>T | NP_005240.3:p.Thr278= | |
| NM_005249.5:c.834C>T MANE Select | NP_005240.3:p.Thr278= |