HGVS | Genome Assembly |
---|---|
NC_000019.10:g.48965260T>G , CM000681.2:g.48965260T>G | GRCh38 |
NC_000019.9:g.49468517T>G , CM000681.1:g.49468517T>G | GRCh37 |
NC_000019.8:g.54160329T>G | NCBI36 |
NG_008152.1:g.4952T>G |
HGVS | Amino-acid Change | |
---|---|---|
XM_024451447.1:c.263T>G | XP_024307215.1:p.Leu88Arg |