Linked Data
dbSNP Id:
rs778317867
gnomAD v3:
10-71834492-C-A
gnomAD v4:
10-71834492-C-A
MyVariant Identifiers:
chr10:g.73594249C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.71834492C>A , CM000672.2:g.71834492C>A | GRCh38 |
| NC_000010.10:g.73594249C>A , CM000672.1:g.73594249C>A | GRCh37 |
| NC_000010.9:g.73264255C>A | NCBI36 |
| NG_009301.1:g.21834G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000394936.8:c.54G>T MANE Select | ENSP00000378394.3:p.Pro18= | |
| ENST00000394934.4:c.54G>T | ENSP00000378392.2:p.Pro18= | |
| ENST00000394936.7:c.54G>T | ENSP00000378394.3:p.Pro18= | |
| ENST00000610929.3:c.54G>T | ENSP00000480857.1:p.Pro18= | |
| NM_001042465.1:c.54G>T | NP_001035930.1:p.Pro18= | |
| NM_001042466.1:c.54G>T | NP_001035931.1:p.Pro18= | |
| NM_002778.2:c.54G>T | NP_002769.1:p.Pro18= | |
| NM_001042465.2:c.54G>T | NP_001035930.1:p.Pro18= | |
| NM_001042466.2:c.54G>T | NP_001035931.1:p.Pro18= | |
| NM_002778.3:c.54G>T | NP_002769.1:p.Pro18= | |
| NM_002778.4:c.54G>T MANE Select | NP_002769.1:p.Pro18= | |
| NM_001042465.3:c.54G>T | NP_001035930.1:p.Pro18= | |
| NM_001042466.3:c.54G>T | NP_001035931.1:p.Pro18= |