HGVS | Genome Assembly |
---|---|
NC_000005.10:g.111071854T>A , CM000667.2:g.111071854T>A | GRCh38 |
NC_000005.9:g.110407552T>A , CM000667.1:g.110407552T>A | GRCh37 |
NC_000005.8:g.110435451T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344895.4:c.-37T>A MANE Select | ENSP00000339804.3:n.-37T>A | |
ENST00000344895.3:c.-37T>A | ENSP00000339804.3:n.-37T>A | |
ENST00000420978.6:c.35-71T>A | ENSP00000399099.2:n.35-71T>A | |
NM_033035.4:c.-37T>A | NP_149024.1:n.-37T>A | |
NR_045089.1:n.1439-71T>A | ||
NM_033035.5:c.-37T>A MANE Select | NP_149024.1:n.-37T>A | |
NR_045089.2:n.1457-71T>A |