HGVS | Genome Assembly |
---|---|
NC_000006.12:g.131890340G>T , CM000668.2:g.131890340G>T | GRCh38 |
NC_000006.11:g.132211480G>T , CM000668.1:g.132211480G>T | GRCh37 |
NC_000006.10:g.132253173G>T | NCBI36 |
NG_008206.1:g.87325G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000684674.1:n.1039-1G>T | ||
ENST00000647893.1:c.2608-1G>T MANE Select | ENSP00000498074.1:n.2608-1G>T | |
ENST00000360971.6:c.2608-1G>T | ENSP00000354238.2:n.2608-1G>T | |
ENST00000513998.5:c.*1445-1G>T | ENSP00000422424.1:n.*1445-1G>T | |
NM_006208.2:c.2608-1G>T | NP_006199.2:n.2608-1G>T | |
XM_011535896.1:c.1498-1G>T | XP_011534198.1:n.1498-1G>T | |
NM_006208.3:c.2608-1G>T MANE Select | NP_006199.2:n.2608-1G>T |