HGVS | Genome Assembly |
---|---|
NC_000017.11:g.34256384_34256385insC , CM000679.2:g.34256384_34256385insC | GRCh38 |
NC_000017.10:g.32583403_32583404insC , CM000679.1:g.32583403_32583404insC | GRCh37 |
NC_000017.9:g.29607516_29607517insC | NCBI36 |
NG_012123.1:g.6108_6109insC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000580907.6:c.*41_*42insC | ENSP00000462156.1:n.*41_*42insC | |
ENST00000624362.2:n.1100_1101insC | ||
ENST00000225831.4:c.194+45_194+46insC MANE Select | ENSP00000225831.4:n.194+45_194+46insC | |
ENST00000580907.5:c.*41_*42insC | ENSP00000462156.1:n.*41_*42insC | |
ENST00000582017.1:n.177_178insC | ||
NM_002982.3:c.194+45_194+46insC | NP_002973.1:n.194+45_194+46insC | |
NM_002982.4:c.194+45_194+46insC MANE Select | NP_002973.1:n.194+45_194+46insC |