HGVS | Genome Assembly |
---|---|
NC_000015.10:g.67066018G>A , CM000677.2:g.67066018G>A | GRCh38 |
NC_000015.9:g.67358356G>A , CM000677.1:g.67358356G>A | GRCh37 |
NC_000015.8:g.65145410G>A | NCBI36 |
NG_011990.1:g.5162G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559460.6:c.-110+2074G>A | ENSP00000453082.2:n.-110+2074G>A | |
ENST00000560424.2:c.-137G>A | ENSP00000455540.2:n.-137G>A | |
ENST00000327367.9:c.-137G>A MANE Select | ENSP00000332973.4:n.-137G>A | |
ENST00000327367.8:c.-137G>A | ENSP00000332973.4:n.-137G>A | |
ENST00000559460.5:c.-110+2074G>A | ENSP00000453082.1:n.-110+2074G>A | |
NM_005902.3:c.-137G>A | NP_005893.1:n.-137G>A | |
XM_011521559.1:c.-137G>A | XP_011519861.1:n.-137G>A | |
NM_005902.4:c.-137G>A MANE Select | NP_005893.1:n.-137G>A |