HGVS | Genome Assembly |
---|---|
NC_000006.12:g.28162011T>G , CM000668.2:g.28162011T>G | GRCh38 |
NC_000006.11:g.28129789T>G , CM000668.1:g.28129789T>G | GRCh37 |
NC_000006.10:g.28237768T>G | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000562227.2:n.53+190T>G | ||
ENST00000440790.6:n.41+190T>G | ||
ENST00000570126.1:n.30+190T>G | ||
NR_103448.1:n.61+190T>G |