HGVS | Genome Assembly |
---|---|
NC_000008.11:g.1296120G>T , CM000670.2:g.1296120G>T | GRCh38 |
NC_000008.10:g.1244380G>T , CM000670.1:g.1244380G>T | GRCh37 |
NC_000008.9:g.1231787G>T | NCBI36 |
NG_009409.2:g.563402G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000421627.7:c.103+37237G>T | ENSP00000400258.3:n.103+37237G>T | |
ENST00000637795.2:c.106+37237G>T MANE Select | ENSP00000489774.1:n.106+37237G>T | |
NR_111948.1:n.2963C>A | ||
XM_011534761.1:c.-135+37237G>T | XP_011533063.1:n.-135+37237G>T | |
XM_011534762.1:c.-135+37237G>T | XP_011533064.1:n.-135+37237G>T | |
NM_001346810.1:c.106+37237G>T | NP_001333739.1:n.106+37237G>T | |
NM_001346810.2:c.106+37237G>T MANE Select | NP_001333739.1:n.106+37237G>T |