HGVS | Genome Assembly |
---|---|
NC_000013.11:g.33024487C>G , CM000675.2:g.33024487C>G | GRCh38 |
NC_000013.10:g.33598625C>G , CM000675.1:g.33598625C>G | GRCh37 |
NC_000013.9:g.32496625C>G | NCBI36 |
NG_011485.1:g.13055C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000380099.4:c.819+7228C>G MANE Select | ENSP00000369442.3:n.819+7228C>G | |
ENST00000380099.3:c.819+7228C>G | ENSP00000369442.3:n.819+7228C>G | |
ENST00000487852.1:n.827+7228C>G | ||
NM_004795.3:c.819+7228C>G | NP_004786.2:n.819+7228C>G | |
XM_006719895.1:c.-103+8174C>G | XP_006719958.1:n.-103+8174C>G | |
XM_006719895.2:c.-103+8174C>G | XP_006719958.1:n.-103+8174C>G | |
NM_004795.4:c.819+7228C>G MANE Select | NP_004786.2:n.819+7228C>G |