Linked Data
ClinVar Variation Id:
2994488
ClinVar RCV Id:
RCV003856127
MyVariant Identifiers:
chr15:g.73614870A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73322529A>G , CM000677.2:g.73322529A>G | GRCh38 |
| NC_000015.9:g.73614870A>G , CM000677.1:g.73614870A>G | GRCh37 |
| NC_000015.8:g.71401923A>G | NCBI36 |
| NG_009063.1:g.51736T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261917.4:c.3564T>C MANE Select | ENSP00000261917.3:p.Pro1188= | |
| ENST00000261917.3:c.3564T>C | ENSP00000261917.3:p.Pro1188= | |
| NM_005477.2:c.3564T>C | NP_005468.1:p.Pro1188= | |
| XM_011521148.1:c.2346T>C | XP_011519450.1:p.Pro782= | |
| XM_011521148.2:c.2346T>C | XP_011519450.1:p.Pro782= | |
| NM_005477.3:c.3564T>C MANE Select | NP_005468.1:p.Pro1188= |