HGVS | Genome Assembly |
---|---|
NC_000006.12:g.38696819G>C , CM000668.2:g.38696819G>C | GRCh38 |
NC_000006.11:g.38664595G>C , CM000668.1:g.38664595G>C | GRCh37 |
NC_000006.10:g.38772573G>C | NCBI36 |
NG_012074.1:g.11358C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373365.5:c.84+6152C>G MANE Select | ENSP00000362463.3:n.84+6152C>G | |
ENST00000373365.4:c.84+6152C>G | ENSP00000362463.3:n.84+6152C>G | |
NM_006708.2:c.84+6152C>G | NP_006699.2:n.84+6152C>G | |
NM_006708.3:c.84+6152C>G MANE Select | NP_006699.2:n.84+6152C>G |