HGVS | Genome Assembly |
---|---|
NC_000005.10:g.157109297C>A , CM000667.2:g.157109297C>A | GRCh38 |
NC_000005.9:g.156536308C>A , CM000667.1:g.156536308C>A | GRCh37 |
NC_000005.8:g.156468886C>A | NCBI36 |
NG_030444.1:g.4941G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000524219.2:c.-293-2335G>T | ENSP00000430328.2:n.-293-2335G>T | |
ENST00000696899.1:c.-264-50G>T | ENSP00000512960.1:n.-264-50G>T | |
ENST00000696901.1:c.-314G>T | ENSP00000512962.1:n.-314G>T | |
ENST00000307851.8:c.-314G>T | ENSP00000312002.4:n.-314G>T | |
ENST00000524219.1:c.-293-2335G>T | ENSP00000430328.1:n.-293-2335G>T |