HGVS | Genome Assembly |
---|---|
NC_000017.11:g.13573767G>A , CM000679.2:g.13573767G>A | GRCh38 |
NC_000017.10:g.13477084G>A , CM000679.1:g.13477084G>A | GRCh37 |
NC_000017.9:g.13417809G>A | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000284110.2:c.599+26764C>T MANE Select | ENSP00000284110.1:n.599+26764C>T | |
ENST00000284110.1:c.599+26764C>T | ENSP00000284110.1:n.599+26764C>T | |
NM_006042.2:c.599+26764C>T | NP_006033.1:n.599+26764C>T | |
NM_006042.3:c.599+26764C>T MANE Select | NP_006033.1:n.599+26764C>T |