Linked Data
dbSNP Id:
rs1582022359
gnomAD v4:
5-179833658-C-T
MyVariant Identifiers:
chr5:g.179260658C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.179833658C>T , CM000667.2:g.179833658C>T | GRCh38 |
| NC_000005.9:g.179260658C>T , CM000667.1:g.179260658C>T | GRCh37 |
| NC_000005.8:g.179193264C>T | NCBI36 |
| NG_011342.1:g.32271C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389805.9:c.1041C>T MANE Select | ENSP00000374455.4:p.Asp347= | |
| ENST00000360718.5:c.789C>T | ENSP00000353944.5:p.Asp263= | |
| ENST00000389805.8:c.1041C>T | ENSP00000374455.4:p.Asp347= | |
| ENST00000510187.5:c.950+431C>T | ENSP00000424477.1:n.950+431C>T | |
| NM_001142298.1:c.789C>T | NP_001135770.1:p.Asp263= | |
| NM_001142299.1:c.789C>T | NP_001135771.1:p.Asp263= | |
| NM_003900.4:c.1041C>T | NP_003891.1:p.Asp347= | |
| XM_017010010.1:c.789C>T | XP_016865499.1:p.Asp263= | |
| NM_003900.5:c.1041C>T MANE Select | NP_003891.1:p.Asp347= | |
| NM_001142298.2:c.789C>T | NP_001135770.1:p.Asp263= | |
| NM_001142299.2:c.789C>T | NP_001135771.1:p.Asp263= |