Linked Data
ClinVar Variation Id:
357667
ClinVar RCV Id:
RCV000390945
dbSNP Id:
rs886061659
gnomAD v4:
6-6145577-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.6145577C>T , CM000668.2:g.6145577C>T | GRCh38 |
| NC_000006.11:g.6145810C>T , CM000668.1:g.6145810C>T | GRCh37 |
| NC_000006.10:g.6090809C>T | NCBI36 |
| NG_008107.1:g.180115G>A , LRG_549:g.180115G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000264870.8:c.*42G>A MANE Select | ENSP00000264870.3:n.*42G>A | |
| ENST00000264870.7:c.*42G>A | ENSP00000264870.3:n.*42G>A | |
| NM_000129.3:c.*42G>A , LRG_549t1:c.*42G>A | NP_000120.2:n.*42G>A | |
| XM_006715010.2:c.*42G>A | XP_006715073.1:n.*42G>A | |
| XM_011514342.1:c.*42G>A | XP_011512644.1:n.*42G>A | |
| NM_000129.4:c.*42G>A MANE Select | NP_000120.2:n.*42G>A |