HGVS | Genome Assembly |
---|---|
NC_000009.12:g.22115016G>T , CM000671.2:g.22115016G>T | GRCh38 |
NC_000009.11:g.22115015G>T , CM000671.1:g.22115015G>T | GRCh37 |
NC_000009.10:g.22105015G>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
NR_003529.3:n.2908+1217G>T | ||
NR_047532.1:n.1697+1217G>T | ||
NR_047534.1:n.961+1217G>T | ||
NR_047535.1:n.856+2621G>T | ||
NR_047536.1:n.720+2621G>T | ||
NR_047537.1:n.781-5184G>T | ||
NR_047538.1:n.645-5184G>T | ||
NR_047543.1:n.990+1217G>T | ||
NR_120536.1:n.645-5488G>T |