Linked Data
dbSNP Id:
rs1166604204
gnomAD v4:
7-73683427-G-C
MyVariant Identifiers:
chr7:g.73683427G>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.73683427G>C , CM000669.2:g.73683427G>C | GRCh38 |
| NC_000007.13:g.73097757G>C , CM000669.1:g.73097757G>C | GRCh37 |
| NC_000007.12:g.72735693G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395176.3:c.-4C>G (DNAJC30) MANE Select | ENSP00000378605.1:n.-4C>G | |
| ENST00000395176.2:c.-4C>G (DNAJC30) | ENSP00000378605.1:n.-4C>G | |
| ENST00000464615.1:n.359+44G>C (BUD23) | ||
| NM_032317.2:c.-4C>G (DNAJC30) | NP_115693.2:n.-4C>G | |
| NM_032317.3:c.-4C>G (DNAJC30) MANE Select | NP_115693.2:n.-4C>G |