Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.4816310C>T , CM000681.2:g.4816310C>T | GRCh38 |
| NC_000019.9:g.4816322C>T , CM000681.1:g.4816322C>T | GRCh37 |
| NC_000019.8:g.4767322C>T | NCBI36 |
| NG_031998.1:g.20433G>A , LRG_358:g.20433G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248244.6:c.2068G>A MANE Select | ENSP00000248244.4:p.Gly690Arg | |
| ENST00000248244.5:c.2068G>A | ENSP00000248244.4:p.Gly690Arg | |
| ENST00000621756.1:c.1570G>A | ENSP00000479467.1:p.Gly524Arg | |
| NM_182919.3:c.2068G>A , LRG_358t1:c.2068G>A | NP_891549.1:p.Gly690Arg | |
| NM_001385678.1:c.2026G>A | NP_001372607.1:p.Gly676Arg | |
| NM_001385679.1:c.1933G>A | NP_001372608.1:p.Gly645Arg | |
| NM_001385680.1:c.1426G>A | NP_001372609.1:p.Gly476Arg | |
| NM_182919.4:c.2068G>A MANE Select | NP_891549.1:p.Gly690Arg |