Linked Data
ClinVar Variation Id:
410384
ClinVar RCV Id:
RCV000456535
dbSNP Id:
rs542881762
gnomAD v4:
1-173907528-C-T
ERepo:
CA16609956/MONDO:0013144/084
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.173907528C>T , CM000663.2:g.173907528C>T | GRCh38 |
| NC_000001.10:g.173876666C>T , CM000663.1:g.173876666C>T | GRCh37 |
| NC_000001.9:g.172143289C>T | NCBI36 |
| NG_012462.1:g.14851G>A , LRG_577:g.14851G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367698.4:c.1154-14G>A MANE Select | ENSP00000356671.3:n.1154-14G>A | |
| ENST00000367698.3:c.1154-14G>A | ENSP00000356671.3:n.1154-14G>A | |
| ENST00000617423.4:c.560-35G>A | ENSP00000478688.1:n.560-35G>A | |
| NM_000488.3:c.1154-14G>A , LRG_577t1:c.1154-14G>A | NP_000479.1:n.1154-14G>A | |
| XM_005245198.2:c.1010-14G>A | XP_005245255.1:n.1010-14G>A | |
| NM_001365052.1:c.1010-14G>A | NP_001351981.1:n.1010-14G>A | |
| NM_000488.4:c.1154-14G>A MANE Select | NP_000479.1:n.1154-14G>A | |
| NM_001365052.2:c.1010-14G>A | NP_001351981.1:n.1010-14G>A | |
| NM_001386302.1:c.1277-14G>A | NP_001373231.1:n.1277-14G>A | |
| NM_001386303.1:c.1235-14G>A | NP_001373232.1:n.1235-14G>A | |
| NM_001386304.1:c.1133-14G>A | NP_001373233.1:n.1133-14G>A | |
| NM_001386305.1:c.1097-14G>A | NP_001373234.1:n.1097-14G>A | |
| NM_001386306.1:c.938-14G>A | NP_001373235.1:n.938-14G>A |