HGVS | Genome Assembly |
---|---|
NC_000011.10:g.46827777del , CM000673.2:g.46827777del | GRCh38 |
NC_000011.9:g.46849328del , CM000673.1:g.46849328del | GRCh37 |
NC_000011.8:g.46805904del | NCBI36 |
NG_029924.1:g.23532del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000529230.6:c.-37-6509del MANE Select | ENSP00000432768.1:n.-37-6509del | |
ENST00000312055.9:c.-37-6509del | ENSP00000310227.5:n.-37-6509del | |
ENST00000525248.1:n.78-6529del | ||
ENST00000529230.5:c.-37-6509del | ENSP00000432768.1:n.-37-6509del | |
NM_001008938.3:c.-37-6509del | NP_001008938.1:n.-37-6509del | |
NM_014756.3:c.-37-6509del | NP_055571.2:n.-37-6509del | |
NM_001008938.4:c.-37-6509del MANE Select | NP_001008938.1:n.-37-6509del | |
NM_014756.4:c.-37-6509del | NP_055571.2:n.-37-6509del |