HGVS | Genome Assembly |
---|---|
NC_000019.10:g.40285500A>G , CM000681.2:g.40285500A>G | GRCh38 |
NC_000019.9:g.40791407A>G , CM000681.1:g.40791407A>G | GRCh37 |
NC_000019.8:g.45483247A>G | NCBI36 |
NG_012038.2:g.4859T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000578123.5:c.-137T>C | ENSP00000462022.1:n.-137T>C | |
XM_011526620.1:c.-137T>C | XP_011524922.1:n.-137T>C |