HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94949198T>C , CM000672.2:g.94949198T>C | GRCh38 |
NC_000010.10:g.96708955T>C , CM000672.1:g.96708955T>C | GRCh37 |
NC_000010.9:g.96698945T>C | NCBI36 |
NG_008385.1:g.15541T>C | |
NG_008385.2:g.16041T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000260682.8:c.733T>C MANE Select | ENSP00000260682.6:p.Leu245= | |
ENST00000643112.1:c.733T>C | ENSP00000496202.1:p.Leu245= | |
ENST00000260682.6:c.733T>C | ENSP00000260682.6:p.Leu245= | |
ENST00000473496.1:n.504T>C | ||
NM_000771.3:c.733T>C | NP_000762.2:p.Leu245= | |
NM_000771.4:c.733T>C MANE Select | NP_000762.2:p.Leu245= |