Linked Data
ClinVar Variation Id:
1997494
ClinVar RCV Id:
RCV002824038
MyVariant Identifiers:
chr10:g.73594255G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.71834498G>T , CM000672.2:g.71834498G>T | GRCh38 |
| NC_000010.10:g.73594255G>T , CM000672.1:g.73594255G>T | GRCh37 |
| NC_000010.9:g.73264261G>T | NCBI36 |
| NG_009301.1:g.21828C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000394936.8:c.48C>A MANE Select | ENSP00000378394.3:p.Ala16= | |
| ENST00000394934.4:c.48C>A | ENSP00000378392.2:p.Ala16= | |
| ENST00000394936.7:c.48C>A | ENSP00000378394.3:p.Ala16= | |
| ENST00000610929.3:c.48C>A | ENSP00000480857.1:p.Ala16= | |
| NM_001042465.1:c.48C>A | NP_001035930.1:p.Ala16= | |
| NM_001042466.1:c.48C>A | NP_001035931.1:p.Ala16= | |
| NM_002778.2:c.48C>A | NP_002769.1:p.Ala16= | |
| NM_001042465.2:c.48C>A | NP_001035930.1:p.Ala16= | |
| NM_001042466.2:c.48C>A | NP_001035931.1:p.Ala16= | |
| NM_002778.3:c.48C>A | NP_002769.1:p.Ala16= | |
| NM_002778.4:c.48C>A MANE Select | NP_002769.1:p.Ala16= | |
| NM_001042465.3:c.48C>A | NP_001035930.1:p.Ala16= | |
| NM_001042466.3:c.48C>A | NP_001035931.1:p.Ala16= |