Linked Data
ClinVar Variation Id:
2879549
ClinVar RCV Id:
RCV003710800
gnomAD v4:
1-146019454-G-A
MyVariant Identifiers:
chr1:g.145415559C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.146019454G>A , CM000663.2:g.146019454G>A | GRCh38 |
| NC_000001.10:g.145415559C>T , CM000663.1:g.145415559C>T | GRCh37 |
| NC_000001.9:g.144126916C>T | NCBI36 |
| NG_011568.1:g.7369C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000336751.11:c.378C>T MANE Select | ENSP00000337014.5:p.Ala126= | |
| ENST00000636675.1:c.-22+244C>T | ENSP00000490072.1:n.-22+244C>T | |
| ENST00000336751.10:c.378C>T | ENSP00000337014.5:p.Ala126= | |
| ENST00000357836.5:c.39C>T | ENSP00000350495.5:p.Ala13= | |
| ENST00000475797.1:c.-21-754C>T | ENSP00000425716.1:n.-21-754C>T | |
| ENST00000497365.5:c.-22+244C>T | ENSP00000421820.1:n.-22+244C>T | |
| ENST00000634927.1:c.134+244C>T | ENSP00000489347.1:n.134+244C>T | |
| NM_001316767.1:c.-22+244C>T | NP_001303696.1:n.-22+244C>T | |
| NM_145277.4:c.39C>T | NP_660320.3:p.Ala13= | |
| NM_202004.3:c.-22+244C>T | NP_973733.1:n.-22+244C>T | |
| NM_213652.3:c.-21-754C>T | NP_998817.1:n.-21-754C>T | |
| NM_213653.3:c.378C>T | NP_998818.1:p.Ala126= | |
| XM_005272932.1:c.378C>T | XP_005272989.1:p.Ala126= | |
| NM_001316767.2:c.-22+244C>T | NP_001303696.1:n.-22+244C>T | |
| NM_145277.5:c.39C>T | NP_660320.3:p.Ala13= | |
| NM_202004.4:c.-22+244C>T | NP_973733.1:n.-22+244C>T | |
| NM_213652.4:c.-21-754C>T | NP_998817.1:n.-21-754C>T | |
| NM_001379352.1:c.378C>T | NP_001366281.1:p.Ala126= | |
| NM_213653.4:c.378C>T MANE Select | NP_998818.1:p.Ala126= |