HGVS | Genome Assembly |
---|---|
NC_000019.10:g.48965243T>C , CM000681.2:g.48965243T>C | GRCh38 |
NC_000019.9:g.49468500T>C , CM000681.1:g.49468500T>C | GRCh37 |
NC_000019.8:g.54160312T>C | NCBI36 |
NG_008152.1:g.4935T>C |
HGVS | Amino-acid Change | |
---|---|---|
XM_024451447.1:c.246T>C | XP_024307215.1:p.Pro82= |