HGVS | Genome Assembly |
---|---|
NC_000005.10:g.111071738_111071740dup , CM000667.2:g.111071738_111071740dup | GRCh38 |
NC_000005.9:g.110407436_110407438dup , CM000667.1:g.110407436_110407438dup | GRCh37 |
NC_000005.8:g.110435335_110435337dup | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344895.4:c.-153_-151dup MANE Select | ENSP00000339804.3:n.-153_-151dup | |
ENST00000344895.3:c.-153_-151dup | ENSP00000339804.3:n.-153_-151dup | |
ENST00000420978.6:c.35-187_35-185dup | ENSP00000399099.2:n.35-187_35-185dup | |
NM_033035.4:c.-153_-151dup | NP_149024.1:n.-153_-151dup | |
NR_045089.1:n.1439-187_1439-185dup | ||
NM_033035.5:c.-153_-151dup MANE Select | NP_149024.1:n.-153_-151dup | |
NR_045089.2:n.1457-187_1457-185dup |