Linked Data
dbSNP Id:
rs1331327912
gnomAD v2:
22-51160515-C-T
gnomAD v3:
22-50722087-C-T
gnomAD v4:
22-50722087-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.50722087C>T , CM000684.2:g.50722087C>T | GRCh38 |
| NC_000022.10:g.51160515C>T , CM000684.1:g.51160515C>T | GRCh37 |
| NC_000022.9:g.49507381C>T | NCBI36 |
| NG_008607.2:g.52733C>T | |
| NG_070230.1:g.57871C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262795.7:c.3855C>T | ENSP00000489147.2:p.Leu1285= | |
| ENST00000414786.7:n.4439C>T | ||
| ENST00000445220.7:c.2907C>T | ENSP00000489407.2:p.Leu969= | |
| ENST00000664402.2:c.2397C>T | ENSP00000499475.1:p.Leu799= | |
| ENST00000673971.2:c.*2853C>T | ENSP00000501192.1:n.*2853C>T | |
| ENST00000445220.6:c.2907C>T | ENSP00000489407.2:p.Leu969= | |
| ENST00000262795.6:c.3855C>T | ENSP00000489147.2:p.Leu1285= | |
| ENST00000664402.1:c.2397C>T | ENSP00000499475.1:p.Leu799= | |
| ENST00000673971.1:c.*2853C>T | ENSP00000501192.1:n.*2853C>T | |
| ENST00000262795.5:c.4251C>T | ENSP00000489147.1:p.Leu1417= | |
| ENST00000414786.6:n.4439C>T | ||
| ENST00000445220.5:c.4233C>T | ENSP00000489407.1:p.Leu1411= |