HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48503787del , CM000677.2:g.48503787del | GRCh38 |
NC_000015.9:g.48795984del , CM000677.1:g.48795984del | GRCh37 |
NC_000015.8:g.46583276del | NCBI36 |
NG_008805.2:g.147003del , LRG_778:g.147003del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559133.6:c.2113+1del | ||
ENST00000674301.2:c.2113+1del | ||
ENST00000684448.1:n.787+1del | ||
ENST00000316623.10:c.2113+1del | ||
ENST00000316623.9:c.2113+1del | ||
ENST00000537463.6:c.637-29136del | ENSP00000440294.2:n.637-29136del | |
NM_000138.4:c.2113+1del , LRG_778t1:c.2113+1del | ||
NM_000138.5:c.2113+1del |