HGVS | Genome Assembly |
---|---|
NC_000006.12:g.160009752T>C , CM000668.2:g.160009752T>C | GRCh38 |
NC_000006.11:g.160430784T>C , CM000668.1:g.160430784T>C | GRCh37 |
NC_000006.10:g.160350774T>C | NCBI36 |
NG_011785.3:g.45654T>C | |
NG_011785.4:g.45654T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000356956.6:c.414+618T>C MANE Select | ENSP00000349437.1:n.414+618T>C | |
ENST00000676781.1:c.414+618T>C | ENSP00000504419.1:n.414+618T>C | |
ENST00000677704.1:c.414+618T>C | ENSP00000503314.1:n.414+618T>C | |
ENST00000356956.5:c.414+618T>C | ENSP00000349437.1:n.414+618T>C | |
NM_000876.2:c.414+618T>C | NP_000867.2:n.414+618T>C | |
XR_942419.1:n.429+618T>C | ||
NM_000876.3:c.414+618T>C | NP_000867.2:n.414+618T>C | |
NM_000876.4:c.414+618T>C MANE Select | NP_000867.3:n.414+618T>C |