HGVS | Genome Assembly |
---|---|
NC_000006.12:g.28161873G>T , CM000668.2:g.28161873G>T | GRCh38 |
NC_000006.11:g.28129651G>T , CM000668.1:g.28129651G>T | GRCh37 |
NC_000006.10:g.28237630G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000562227.2:n.53+52G>T | ||
ENST00000440790.6:n.41+52G>T | ||
ENST00000570126.1:n.30+52G>T | ||
NR_103448.1:n.61+52G>T |