HGVS | Genome Assembly |
---|---|
NC_000005.10:g.157109246T>A , CM000667.2:g.157109246T>A | GRCh38 |
NC_000005.9:g.156536257T>A , CM000667.1:g.156536257T>A | GRCh37 |
NC_000005.8:g.156468835T>A | NCBI36 |
NG_030444.1:g.4992A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000524219.2:c.-293-2284A>T | ENSP00000430328.2:n.-293-2284A>T | |
ENST00000696899.1:c.-263A>T | ENSP00000512960.1:n.-263A>T | |
ENST00000696900.1:c.-858A>T | ENSP00000512961.1:n.-858A>T | |
ENST00000696901.1:c.-263A>T | ENSP00000512962.1:n.-263A>T | |
ENST00000307851.8:c.-263A>T | ENSP00000312002.4:n.-263A>T | |
ENST00000524219.1:c.-293-2284A>T | ENSP00000430328.1:n.-293-2284A>T |