HGVS | Genome Assembly |
---|---|
NC_000002.12:g.135859165_135859166insTTA , CM000664.2:g.135859165_135859166insTTA | GRCh38 |
NC_000002.11:g.136616735_136616736insTTA , CM000664.1:g.136616735_136616736insTTA | GRCh37 |
NC_000002.10:g.136333205_136333206insTTA | NCBI36 |
NG_008104.2:g.1005_1006insAAT , LRG_338:g.1005_1006insAAT | |
NG_008958.1:g.22277_22278insAAT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264156.3:c.1362+136_1362+137insAAT MANE Select | ENSP00000264156.2:n.1362+136_1362+137insAAT | |
ENST00000264156.2:c.1362+136_1362+137insAAT | ENSP00000264156.2:n.1362+136_1362+137insAAT | |
ENST00000492091.1:n.181+3442_181+3443insAAT | ||
NM_005915.5:c.1362+136_1362+137insAAT | NP_005906.2:n.1362+136_1362+137insAAT | |
NM_005915.6:c.1362+136_1362+137insAAT MANE Select | NP_005906.2:n.1362+136_1362+137insAAT |