Linked Data
dbSNP Id:
rs543422060
gnomAD v3:
10-94942098-G-C
gnomAD v4:
10-94942098-G-C
MyVariant Identifiers:
chr10:g.94942098G>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94942098G>C , CM000672.2:g.94942098G>C | GRCh38 |
| NC_000010.10:g.96701855G>C , CM000672.1:g.96701855G>C | GRCh37 |
| NC_000010.9:g.96691845G>C | NCBI36 |
| NG_008385.1:g.8441G>C | |
| NG_008385.2:g.8941G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000260682.8:c.331+78G>C MANE Select | ENSP00000260682.6:n.331+78G>C | |
| ENST00000643112.1:c.331+78G>C | ENSP00000496202.1:n.331+78G>C | |
| ENST00000645207.1:n.484+78G>C | ||
| ENST00000260682.6:c.331+78G>C | ENSP00000260682.6:n.331+78G>C | |
| ENST00000461906.1:n.356+78G>C | ||
| ENST00000473496.1:n.102+78G>C | ||
| NM_000771.3:c.331+78G>C | NP_000762.2:n.331+78G>C | |
| NM_000771.4:c.331+78G>C MANE Select | NP_000762.2:n.331+78G>C |