HGVS | Genome Assembly |
---|---|
NC_000007.14:g.152648413_152648414insGA , CM000669.2:g.152648413_152648414insGA | GRCh38 |
NC_000007.13:g.152345498_152345499insGA , CM000669.1:g.152345498_152345499insGA | GRCh37 |
NC_000007.12:g.151976431_151976432insGA | NCBI36 |
NG_027988.1:g.32752_32753insTC | |
NG_027988.2:g.32752_32753insTC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698506.1:c.*228_*229insTC | ENSP00000513758.1:n.*228_*229insTC | |
ENST00000359321.2:c.*228_*229insTC MANE Select | ENSP00000352271.1:n.*228_*229insTC | |
ENST00000359321.1:c.*228_*229insTC | ENSP00000352271.1:n.*228_*229insTC | |
ENST00000495707.1:n.1093_1094insTC | ||
NM_005431.1:c.*228_*229insTC | NP_005422.1:n.*228_*229insTC | |
NM_005431.2:c.*228_*229insTC MANE Select | NP_005422.1:n.*228_*229insTC |