Linked Data
ClinVar Variation Id:
2699205
ClinVar RCV Id:
RCV003544518
gnomAD v4:
1-216175385-A-T
MyVariant Identifiers:
chr1:g.216348727A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.216175385A>T , CM000663.2:g.216175385A>T | GRCh38 |
| NC_000001.10:g.216348727A>T , CM000663.1:g.216348727A>T | GRCh37 |
| NC_000001.9:g.214415350A>T | NCBI36 |
| NG_009497.1:g.253012T>A | |
| NG_009497.2:g.253064T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.4494T>A MANE Select | ENSP00000305941.3:p.Pro1498= | |
| ENST00000674083.1:c.4494T>A | ENSP00000501296.1:p.Pro1498= | |
| ENST00000307340.7:c.4494T>A | ENSP00000305941.3:p.Pro1498= | |
| ENST00000366942.3:c.4494T>A | ENSP00000355909.3:p.Pro1498= | |
| NM_007123.5:c.4494T>A | NP_009054.5:p.Pro1498= | |
| NM_206933.2:c.4494T>A | NP_996816.2:p.Pro1498= | |
| NM_206933.3:c.4494T>A | NP_996816.2:p.Pro1498= | |
| NM_007123.6:c.4494T>A | NP_009054.6:p.Pro1498= | |
| NM_206933.4:c.4494T>A MANE Select | NP_996816.3:p.Pro1498= |