HGVS | Genome Assembly |
---|---|
NC_000010.11:g.99836460T>A , CM000672.2:g.99836460T>A | GRCh38 |
NC_000010.10:g.101596217T>A , CM000672.1:g.101596217T>A | GRCh37 |
NC_000010.9:g.101586207T>A | NCBI36 |
NG_011798.1:g.58755T>A | |
NG_011798.2:g.58863T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647814.1:c.3614+170T>A MANE Select | ENSP00000497274.1:n.3614+170T>A | |
ENST00000370449.8:c.3614+170T>A | ENSP00000359478.4:n.3614+170T>A | |
NM_000392.4:c.3614+170T>A | NP_000383.1:n.3614+170T>A | |
XM_006717630.2:c.2918+170T>A | XP_006717693.1:n.2918+170T>A | |
XR_945604.1:n.3803+170T>A | ||
XR_945605.1:n.3805+170T>A | ||
NM_000392.5:c.3614+170T>A MANE Select | NP_000383.2:n.3614+170T>A | |
XM_006717630.3:c.2918+170T>A | XP_006717693.1:n.2918+170T>A | |
XR_945604.3:n.3857+170T>A | ||
XR_945605.3:n.3857+170T>A |