Linked Data
dbSNP Id:
rs751074068
ExAC:
19:54403883 T / C
gnomAD v2:
19-54403883-T-C
gnomAD v3:
19-53900629-T-C
gnomAD v4:
19-53900629-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.53900629T>C , CM000681.2:g.53900629T>C | GRCh38 |
| NC_000019.9:g.54403883T>C , CM000681.1:g.54403883T>C | GRCh37 |
| NC_000019.8:g.59095695T>C | NCBI36 |
| NG_009114.1:g.23417T>C , LRG_669:g.23417T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682028.1:c.1455T>C | ENSP00000507230.1:p.Asn485= | |
| ENST00000682268.1:n.1753T>C | ||
| ENST00000682676.1:n.856T>C | ||
| ENST00000682902.1:n.1757T>C | ||
| ENST00000683513.1:c.1455T>C | ENSP00000506809.1:p.Asn485= | |
| ENST00000263431.4:c.1455T>C MANE Select | ENSP00000263431.3:p.Asn485= | |
| ENST00000263431.3:c.1455T>C | ENSP00000263431.3:p.Asn485= | |
| NM_001316329.1:c.1455T>C | NP_001303258.1:p.Asn485= | |
| NM_002739.3:c.1455T>C , LRG_669t1:c.1455T>C | NP_002730.1:p.Asn485= | |
| NM_002739.4:c.1455T>C | NP_002730.1:p.Asn485= | |
| XM_011527108.1:c.546T>C | XP_011525410.1:p.Asn182= | |
| NM_002739.5:c.1455T>C MANE Select | NP_002730.1:p.Asn485= | |
| NM_001316329.2:c.1455T>C | NP_001303258.1:p.Asn485= |