HGVS | Genome Assembly |
---|---|
NC_000020.11:g.10644722C>T , CM000682.2:g.10644722C>T | GRCh38 |
NC_000020.10:g.10625370C>T , CM000682.1:g.10625370C>T | GRCh37 |
NC_000020.9:g.10573370C>T | NCBI36 |
NG_007496.1:g.34325G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000254958.10:c.2344+141G>A MANE Select | ENSP00000254958.4:n.2344+141G>A | |
ENST00000617965.2:n.2933+141G>A | ||
ENST00000254958.9:c.2344+141G>A | ENSP00000254958.4:n.2344+141G>A | |
ENST00000423891.6:n.2210+141G>A | ||
ENST00000488480.2:n.882G>A | ||
NM_000214.2:c.2344+141G>A | NP_000205.1:n.2344+141G>A | |
NM_000214.3:c.2344+141G>A MANE Select | NP_000205.1:n.2344+141G>A |