HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32819184A>G , CM000668.2:g.32819184A>G | GRCh38 |
NC_000006.11:g.32786961A>G , CM000668.1:g.32786961A>G | GRCh37 |
NC_000006.10:g.32894939A>G | NCBI36 |
NG_009793.3:g.24587T>C | |
NG_012008.1:g.2865T>C | |
NG_009793.4:g.24587T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000648009.1:c.-2+1127T>C | ENSP00000496848.1:n.-2+1127T>C | |
ENST00000452392.2:c.1933-2232T>C | ENSP00000391806.2:n.1933-2232T>C |