HGVS | Genome Assembly |
---|---|
NC_000009.12:g.119297431T>C , CM000671.2:g.119297431T>C | GRCh38 |
NC_000009.11:g.122059709T>C , CM000671.1:g.122059709T>C | GRCh37 |
NC_000009.10:g.121099530T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000265922.8:c.218+15707A>G MANE Select | ENSP00000265922.2:n.218+15707A>G | |
ENST00000265922.7:c.218+15707A>G | ENSP00000265922.2:n.218+15707A>G | |
ENST00000373964.2:c.218+15707A>G | ENSP00000363075.1:n.218+15707A>G | |
NM_014618.2:c.218+15707A>G | NP_055433.2:n.218+15707A>G | |
NM_014618.3:c.218+15707A>G MANE Select | NP_055433.2:n.218+15707A>G |