Linked Data
ClinVar Variation Id:
1534337
ClinVar RCV Id:
RCV002076693
dbSNP Id:
rs770431439
gnomAD v3:
1-45500410-C-T
gnomAD v4:
1-45500410-C-T
MyVariant Identifiers:
chr1:g.45966082C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.45500410C>T , CM000663.2:g.45500410C>T | GRCh38 |
| NC_000001.10:g.45966082C>T , CM000663.1:g.45966082C>T | GRCh37 |
| NC_000001.9:g.45738669C>T | NCBI36 |
| NG_013378.1:g.5227C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000401061.9:c.78C>T MANE Select | ENSP00000383840.4:p.Phe26= | |
| ENST00000401061.8:c.78C>T | ENSP00000383840.4:p.Phe26= | |
| ENST00000616135.1:c.-94C>T | ENSP00000478859.1:n.-94C>T | |
| NM_015506.2:c.78C>T | NP_056321.2:p.Phe26= | |
| XM_005270724.3:c.78C>T | XP_005270781.1:p.Phe26= | |
| XM_011541204.1:c.-145C>T | XP_011539506.1:n.-145C>T | |
| NM_001330540.1:c.-145C>T | NP_001317469.1:n.-145C>T | |
| XM_005270724.5:c.78C>T | XP_005270781.1:p.Phe26= | |
| NM_015506.3:c.78C>T MANE Select | NP_056321.2:p.Phe26= | |
| NM_001330540.2:c.-145C>T | NP_001317469.1:n.-145C>T |