HGVS | Genome Assembly |
---|---|
NC_000019.10:g.45766621A>G , CM000681.2:g.45766621A>G | GRCh38 |
NC_000019.9:g.46269879A>G , CM000681.1:g.46269879A>G | GRCh37 |
NC_000019.8:g.50961719A>G | NCBI36 |
NG_012745.1:g.7619T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000317578.7:c.1338T>C MANE Select | ENSP00000316842.4:p.Pro446= | |
ENST00000317578.6:c.1338T>C | ENSP00000316842.4:p.Pro446= | |
ENST00000560160.1:c.587-510T>C | ||
ENST00000560168.1:c.*526T>C | ENSP00000453189.2:n.*526T>C | |
ENST00000622857.1:c.16-659T>C | ENSP00000481365.1:n.16-659T>C | |
NM_175875.4:c.1338T>C | NP_787071.2:p.Pro446= | |
NM_175875.5:c.1338T>C MANE Select | NP_787071.3:p.Pro446= |