HGVS | Genome Assembly |
---|---|
NC_000007.14:g.150851761G= , CM000669.2:g.150851761G= | GRCh38 |
NC_000007.13:g.150548849G= , CM000669.1:g.150548849G= | GRCh37 |
NC_000007.12:g.150179782G= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000467291.5:c.-92-354G= | ENSP00000418328.1:n.-92-354G= | |
ENST00000493429.5:c.-92-354G= | ENSP00000418614.1:n.-92-354G= | |
XM_011516008.1:c.-181-354G= | XP_011514310.1:n.-181-354G= | |
XM_011516009.1:c.-92-354G= | XP_011514311.1:n.-92-354G= | |
XR_928169.1:n.296-10316C= | ||
XR_928170.1:n.426-10316C= | ||
XR_928171.1:n.298-10316C= | ||
XM_017011944.1:c.-92-354G= | XP_016867433.1:n.-92-354G= | |
XM_017011945.1:c.-92-354G= | XP_016867434.1:n.-92-354G= | |
XR_928169.2:n.302-10316C= | ||
XR_928171.2:n.302-10316C= |