HGVS | Genome Assembly |
---|---|
NC_000010.11:g.99845804G= , CM000672.2:g.99845804G= | GRCh38 |
NC_000010.10:g.101605561G= , CM000672.1:g.101605561G= | GRCh37 |
NC_000010.9:g.101595551G= | NCBI36 |
NG_011798.1:g.68099G= | |
NG_011798.2:g.68207G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647814.1:c.4146+22G= MANE Select | ENSP00000497274.1:n.4146+22G= | |
ENST00000648523.1:c.34+22G= | ||
ENST00000649459.1:n.494+22G= | ||
ENST00000370449.8:c.4146+22G= | ENSP00000359478.4:n.4146+22G= | |
NM_000392.4:c.4146+22G= | NP_000383.1:n.4146+22G= | |
XM_006717630.2:c.3450+22G= | XP_006717693.1:n.3450+22G= | |
XR_945604.1:n.4276+22G= | ||
XR_945605.1:n.4210+22G= | ||
NM_000392.5:c.4146+22G= MANE Select | NP_000383.2:n.4146+22G= | |
XM_006717630.3:c.3450+22G= | XP_006717693.1:n.3450+22G= | |
XR_945604.3:n.4330+22G= | ||
XR_945605.3:n.4262+22G= |