Linked Data
ClinVar Variation Id:
565920
ClinVar RCV Id:
RCV000685600
dbSNP Id:
rs755106109
ExAC:
2:220283645 T / A
gnomAD v2:
2-220283645-T-A
gnomAD v4:
2-219418923-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.219418923T>A , CM000664.2:g.219418923T>A | GRCh38 |
| NC_000002.11:g.220283645T>A , CM000664.1:g.220283645T>A | GRCh37 |
| NC_000002.10:g.219991889T>A | NCBI36 |
| NG_008043.1:g.5547T>A , LRG_380:g.5547T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373960.4:c.461T>A MANE Select | ENSP00000363071.3:p.Leu154His | |
| ENST00000373960.3:c.461T>A | ENSP00000363071.3:p.Leu154His | |
| NM_001927.3:c.461T>A , LRG_380t1:c.461T>A | NP_001918.3:p.Leu154His | |
| NM_001927.4:c.461T>A MANE Select | NP_001918.3:p.Leu154His | |
| NM_001382708.1:c.461T>A | NP_001369637.1:p.Leu154His | |
| NM_001382709.1:c.461T>A | NP_001369638.1:p.Leu154His | |
| NM_001382710.1:c.461T>A | NP_001369639.1:p.Leu154His | |
| NM_001382711.1:c.461T>A | NP_001369640.1:p.Leu154His | |
| NM_001382712.1:c.461T>A | NP_001369641.1:p.Leu154His | |
| NM_001382713.1:c.461T>A | NP_001369642.1:p.Leu154His |