HGVS | Genome Assembly |
---|---|
NC_000002.12:g.135856685_135856686insGAGT , CM000664.2:g.135856685_135856686insGAGT | GRCh38 |
NC_000002.11:g.136614255_136614256insGAGT , CM000664.1:g.136614255_136614256insGAGT | GRCh37 |
NC_000002.10:g.136330725_136330726insGAGT | NCBI36 |
NG_008104.2:g.3484_3485insACTC , LRG_338:g.3484_3485insACTC | |
NG_008958.1:g.24756_24757insACTC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264156.3:c.1626+42_1626+43insACTC MANE Select | ENSP00000264156.2:n.1626+42_1626+43insACT... | |
ENST00000264156.2:c.1626+42_1626+43insACTC | ENSP00000264156.2:n.1626+42_1626+43insACT... | |
ENST00000492091.1:n.182-5123_182-5122insACTC | ||
NM_005915.5:c.1626+42_1626+43insACTC | NP_005906.2:n.1626+42_1626+43insACTC | |
NM_005915.6:c.1626+42_1626+43insACTC MANE Select | NP_005906.2:n.1626+42_1626+43insACTC |