HGVS | Genome Assembly |
---|---|
NC_000023.11:g.116172075T= , CM000685.2:g.116172075T= | GRCh38 |
NC_000023.10:g.115303328T= , CM000685.1:g.115303328T= | GRCh37 |
NC_000023.9:g.115217356T= | NCBI36 |
NG_016326.1:g.6371T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371906.5:c.-35-171T= MANE Select | ENSP00000360973.4:n.-35-171T= | |
ENST00000680409.1:n.263T= | ||
ENST00000681852.1:c.-35-171T= | ENSP00000505750.1:n.-35-171T= | |
ENST00000371906.4:c.-35-171T= | ENSP00000360973.4:n.-35-171T= | |
NM_000686.4:c.-35-171T= | NP_000677.2:n.-35-171T= | |
XM_011537533.1:c.-35-171T= | XP_011535835.1:n.-35-171T= | |
NM_000686.5:c.-35-171T= MANE Select | NP_000677.2:n.-35-171T= | |
NM_001385624.1:c.-35-171T= | NP_001372553.1:n.-35-171T= |