HGVS | Genome Assembly |
---|---|
NC_000012.12:g.66250294_66250295delinsAT , CM000674.2:g.66250294_66250295delinsAT | GRCh38 |
NC_000012.11:g.66644074_66644075delinsAT , CM000674.1:g.66644074_66644075delinsAT | GRCh37 |
NC_000012.10:g.64930341_64930342delinsAT | NCBI36 |
NG_021194.1:g.66097_66098delinsAT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261233.9:c.*2123_*2124delinsAT MANE Select | ENSP00000261233.4:n.*2123_*2124delinsAT | |
ENST00000261233.8:c.*2123_*2124delinsAT | ENSP00000261233.4:n.*2123_*2124delinsAT | |
NM_001142523.1:c.*2123_*2124delinsAT | NP_001135995.1:n.*2123_*2124delinsAT | |
NM_007199.2:c.*2123_*2124delinsAT | NP_009130.2:n.*2123_*2124delinsAT | |
NM_001142523.2:c.*2123_*2124delinsAT | NP_001135995.1:n.*2123_*2124delinsAT | |
NM_007199.3:c.*2123_*2124delinsAT MANE Select | NP_009130.2:n.*2123_*2124delinsAT |