Linked Data
gnomAD v4:
11-6319488-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6319488C>T , CM000673.2:g.6319488C>T | GRCh38 |
| NC_000011.9:g.6340718C>T , CM000673.1:g.6340718C>T | GRCh37 |
| NC_000011.8:g.6297294C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303927.4:c.461G>A MANE Select | ENSP00000307292.3:p.Gly154Asp | |
| ENST00000303927.3:c.461G>A | ENSP00000307292.3:p.Gly154Asp | |
| ENST00000524852.1:n.247G>A | ||
| ENST00000530979.1:c.557G>A | ENSP00000432047.1:p.Gly186Asp | |
| ENST00000532354.1:n.483G>A | ||
| NM_145040.2:c.461G>A | NP_659477.2:p.Gly154Asp | |
| XR_930997.1:n.720+1268C>T | ||
| XR_001748106.1:n.99C>T | ||
| XR_242848.4:n.348C>T | ||
| NM_145040.3:c.461G>A MANE Select | NP_659477.2:p.Gly154Asp |