HGVS | Genome Assembly |
---|---|
NC_000009.12:g.22115021T>C , CM000671.2:g.22115021T>C | GRCh38 |
NC_000009.11:g.22115020T>C , CM000671.1:g.22115020T>C | GRCh37 |
NC_000009.10:g.22105020T>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
NR_003529.3:n.2908+1222T>C | ||
NR_047532.1:n.1697+1222T>C | ||
NR_047534.1:n.961+1222T>C | ||
NR_047535.1:n.856+2626T>C | ||
NR_047536.1:n.720+2626T>C | ||
NR_047537.1:n.781-5179T>C | ||
NR_047538.1:n.645-5179T>C | ||
NR_047543.1:n.990+1222T>C | ||
NR_120536.1:n.645-5483T>C |