HGVS | Genome Assembly |
---|---|
NC_000001.11:g.28834642G>C , CM000663.2:g.28834642G>C | GRCh38 |
NC_000001.10:g.29161154G>C , CM000663.1:g.29161154G>C | GRCh37 |
NC_000001.9:g.29033741G>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000234961.7:c.227+22032G>C MANE Select | ENSP00000234961.2:n.227+22032G>C | |
ENST00000234961.6:c.227+22032G>C | ENSP00000234961.2:n.227+22032G>C | |
ENST00000621425.1:c.227+22032G>C | ENSP00000477970.1:n.227+22032G>C | |
NM_000911.3:c.227+22032G>C | NP_000902.3:n.227+22032G>C | |
NM_000911.4:c.227+22032G>C MANE Select | NP_000902.3:n.227+22032G>C |