HGVS | Genome Assembly |
---|---|
NC_000001.11:g.114714035A>C , CM000663.2:g.114714035A>C | GRCh38 |
NC_000001.10:g.115256656A>C , CM000663.1:g.115256656A>C | GRCh37 |
NC_000001.9:g.115058179A>C | NCBI36 |
NG_007572.1:g.7860T>G , LRG_92:g.7860T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369535.5:c.112-57T>G MANE Select | ENSP00000358548.4:n.112-57T>G | |
ENST00000369535.4:c.112-57T>G | ENSP00000358548.4:n.112-57T>G | |
NM_002524.4:c.112-57T>G | NP_002515.1:n.112-57T>G | |
NM_002524.5:c.112-57T>G MANE Select | NP_002515.1:n.112-57T>G |