HGVS | Genome Assembly |
---|---|
NC_000007.14:g.106285307C>T , CM000669.2:g.106285307C>T | GRCh38 |
NC_000007.13:g.105925753C>T , CM000669.1:g.105925753C>T | GRCh37 |
NC_000007.12:g.105712989C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000424768.2:c.-98+234G>A | ENSP00000390591.2:n.-98+234G>A | |
ENST00000681255.1:c.-48+234G>A | ENSP00000506129.1:n.-48+234G>A | |
ENST00000681491.1:c.-98+11G>A | ENSP00000506540.1:n.-98+11G>A | |
ENST00000417537.1:c.-48+234G>A | ENSP00000390896.1:n.-48+234G>A | |
ENST00000424768.1:c.-98+234G>A | ENSP00000390591.1:n.-98+234G>A | |
XM_005250100.1:c.-98+234G>A | XP_005250157.1:n.-98+234G>A |