HGVS | Genome Assembly |
---|---|
NC_000009.12:g.74534921A>G , CM000671.2:g.74534921A>G | GRCh38 |
NC_000009.11:g.77149837A>G , CM000671.1:g.77149837A>G | GRCh37 |
NC_000009.10:g.76339657A>G | NCBI36 |
NG_046926.2:g.42586A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376896.8:c.7+36938A>G MANE Select | ENSP00000366093.2:n.7+36938A>G | |
ENST00000376896.7:c.7+36938A>G | ENSP00000366093.2:n.7+36938A>G | |
NM_006914.3:c.7+36938A>G | NP_008845.2:n.7+36938A>G | |
NM_006914.4:c.7+36938A>G MANE Select | NP_008845.2:n.7+36938A>G |