HGVS | Genome Assembly |
---|---|
NC_000019.10:g.48966120T>C , CM000681.2:g.48966120T>C | GRCh38 |
NC_000019.9:g.49469377T>C , CM000681.1:g.49469377T>C | GRCh37 |
NC_000019.8:g.54161189T>C | NCBI36 |
NG_008152.1:g.5812T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331825.11:c.250-161T>C MANE Select | ENSP00000366525.2:n.250-161T>C | |
ENST00000331825.10:c.250-161T>C | ENSP00000366525.2:n.250-161T>C | |
ENST00000622577.2:c.250-161T>C | ENSP00000484043.1:n.250-161T>C | |
NM_000146.3:c.250-161T>C | NP_000137.2:n.250-161T>C | |
XM_024451447.1:c.760-161T>C | XP_024307215.1:n.760-161T>C | |
NM_000146.4:c.250-161T>C MANE Select | NP_000137.2:n.250-161T>C |