Linked Data
dbSNP Id:
rs773348728
ExAC:
14:23902879 C / T
gnomAD v2:
14-23902879-C-T
gnomAD v4:
14-23433670-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23433670C>T , CM000676.2:g.23433670C>T | GRCh38 |
| NC_000014.8:g.23902879C>T , CM000676.1:g.23902879C>T | GRCh37 |
| NC_000014.7:g.22972719C>T | NCBI36 |
| NG_007884.1:g.6992G>A , LRG_384:g.6992G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355349.4:c.63G>A MANE Select | ENSP00000347507.3:p.Lys21= | |
| ENST00000355349.3:c.63G>A | ENSP00000347507.3:p.Lys21= | |
| NM_000257.3:c.63G>A | NP_000248.2:p.Lys21= | |
| XR_245686.3:n.169G>A | ||
| XM_017021340.1:c.63G>A | XP_016876829.1:p.Lys21= | |
| NM_000257.4:c.63G>A MANE Select | NP_000248.2:p.Lys21= |