Linked Data
ClinVar Variation Id:
1657126
ClinVar RCV Id:
RCV002164294
dbSNP Id:
rs2127397406
gnomAD v4:
5-149027827-G-A
MyVariant Identifiers:
chr5:g.148407390G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149027827G>A , CM000667.2:g.149027827G>A | GRCh38 |
| NC_000005.9:g.148407390G>A , CM000667.1:g.148407390G>A | GRCh37 |
| NC_000005.8:g.148387583G>A | NCBI36 |
| NG_007947.2:g.40348C>T , LRG_269:g.40348C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502274.2:c.1801C>T | ||
| ENST00000515425.6:c.1905C>T MANE Select | ENSP00000423660.1:p.Ala635= | |
| ENST00000675793.1:c.*1189C>T | ENSP00000502039.1:n.*1189C>T | |
| ENST00000676056.1:c.*1415C>T | ENSP00000501827.1:n.*1415C>T | |
| ENST00000323829.9:c.*1293C>T | ENSP00000313025.5:n.*1293C>T | |
| ENST00000504517.5:c.1435C>T | ENSP00000421779.1:n.1435C>T | |
| ENST00000504690.5:c.1905C>T | ENSP00000425627.1:p.Ala635= | |
| ENST00000510779.1:c.955C>T | ||
| ENST00000511307.5:c.*1685C>T | ENSP00000421420.1:n.*1685C>T | |
| ENST00000512049.5:c.1884C>T | ENSP00000421860.1:p.Ala628= | |
| ENST00000513604.5:c.*1293C>T | ENSP00000423111.1:n.*1293C>T | |
| ENST00000515425.5:c.1905C>T | ENSP00000423660.1:p.Ala635= | |
| NM_024577.3:c.1905C>T , LRG_269t1:c.1905C>T | NP_078853.2:p.Ala635= | |
| NM_024577.4:c.1905C>T MANE Select | NP_078853.2:p.Ala635= |