HGVS | Genome Assembly |
---|---|
NC_000016.10:g.68737278A>T , CM000678.2:g.68737278A>T | GRCh38 |
NC_000016.9:g.68771181A>T , CM000678.1:g.68771181A>T | GRCh37 |
NC_000016.8:g.67328682A>T | NCBI36 |
NG_008021.1:g.4987A>T , LRG_301:g.4987A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261769.9:c.-138A>T | ENSP00000261769.4:n.-138A>T |