HGVS | Genome Assembly |
---|---|
NC_000001.11:g.154192105A>C , CM000663.2:g.154192105A>C | GRCh38 |
NC_000001.10:g.154164581A>C , CM000663.1:g.154164581A>C | GRCh37 |
NC_000001.9:g.152431205A>C | NCBI36 |
NG_008621.1:g.5029T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000651644.1:c.-87T>G | ENSP00000498648.1:n.-87T>G | |
ENST00000368530.6:c.-87T>G | ENSP00000357516.2:n.-87T>G | |
ENST00000515609.1:c.-49-38T>G | ENSP00000426306.1:n.-49-38T>G | |
NM_152263.3:c.-87T>G | NP_689476.2:n.-87T>G |