HGVS | Genome Assembly |
---|---|
NC_000004.12:g.139873905T>G , CM000666.2:g.139873905T>G | GRCh38 |
NC_000004.11:g.140795059T>G , CM000666.1:g.140795059T>G | GRCh37 |
NC_000004.10:g.141014509T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000502696.1:c.111-143238A>C | ||
ENST00000509479.6:c.2079+15452A>C MANE Select | ENSP00000421180.1:n.2079+15452A>C | |
NM_018717.4:c.2067+15452A>C | NP_061187.2:n.2067+15452A>C | |
NM_018717.5:c.2079+15452A>C MANE Select | NP_061187.3:n.2079+15452A>C |