HGVS | Genome Assembly |
---|---|
NC_000023.11:g.134498351T>C , CM000685.2:g.134498351T>C | GRCh38 |
NC_000023.10:g.133632381T>C , CM000685.1:g.133632381T>C | GRCh37 |
NC_000023.9:g.133460047T>C | NCBI36 |
NG_012329.1:g.43207T>C | |
NG_012329.2:g.43207T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000298556.8:c.486-39T>C MANE Select | ENSP00000298556.7:n.486-39T>C | |
ENST00000298556.7:c.486-39T>C | ENSP00000298556.7:n.486-39T>C | |
ENST00000462974.5:n.644-39T>C | ||
ENST00000475720.1:n.444-39T>C | ||
NM_000194.2:c.486-39T>C | NP_000185.1:n.486-39T>C | |
XM_011531328.1:c.504-39T>C | XP_011529630.1:n.504-39T>C | |
NM_000194.3:c.486-39T>C MANE Select | NP_000185.1:n.486-39T>C |