HGVS | Genome Assembly |
---|---|
NC_000002.12:g.135856540_135856541delinsGT , CM000664.2:g.135856540_135856541delinsGT | GRCh38 |
NC_000002.11:g.136614110_136614111delinsGT , CM000664.1:g.136614110_136614111delinsGT | GRCh37 |
NC_000002.10:g.136330580_136330581delinsGT | NCBI36 |
NG_008104.2:g.3629_3630delinsAC , LRG_338:g.3629_3630delinsAC | |
NG_008958.1:g.24901_24902delinsAC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264156.3:c.1626+187_1626+188delinsAC MANE Select | ENSP00000264156.2:n.1626+187_1626+188delinsAC | |
ENST00000264156.2:c.1626+187_1626+188delinsAC | ENSP00000264156.2:n.1626+187_1626+188delinsAC | |
ENST00000492091.1:n.182-4978_182-4977delinsAC | ||
NM_005915.5:c.1626+187_1626+188delinsAC | NP_005906.2:n.1626+187_1626+188delinsAC | |
NM_005915.6:c.1626+187_1626+188delinsAC MANE Select | NP_005906.2:n.1626+187_1626+188delinsAC |