HGVS | Genome Assembly |
---|---|
NC_000007.14:g.73683430T>A , CM000669.2:g.73683430T>A | GRCh38 |
NC_000007.13:g.73097760T>A , CM000669.1:g.73097760T>A | GRCh37 |
NC_000007.12:g.72735696T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000395176.3:c.-7A>T (DNAJC30) MANE Select | ENSP00000378605.1:n.-7A>T | |
ENST00000395176.2:c.-7A>T (DNAJC30) | ENSP00000378605.1:n.-7A>T | |
ENST00000464615.1:n.359+47T>A (BUD23) | ||
NM_032317.2:c.-7A>T (DNAJC30) | NP_115693.2:n.-7A>T | |
NM_032317.3:c.-7A>T (DNAJC30) MANE Select | NP_115693.2:n.-7A>T |