HGVS | Genome Assembly |
---|---|
NC_000010.11:g.133527154G>T , CM000672.2:g.133527154G>T | GRCh38 |
NC_000010.10:g.135340658G>T , CM000672.1:g.135340658G>T | GRCh37 |
NC_000010.9:g.135190648G>T | NCBI36 |
NG_008383.1:g.4792G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000463117.6:c.-39-203G>T | ENSP00000440689.1:n.-39-203G>T | |
ENST00000541261.1:c.-39-203G>T | ENSP00000437799.1:n.-39-203G>T |