HGVS | Genome Assembly |
---|---|
NC_000008.11:g.10622794_10622881del , CM000670.2:g.10622794_10622881del | GRCh38 |
NC_000008.10:g.10480304_10480391del , CM000670.1:g.10480304_10480391del | GRCh37 |
NC_000008.9:g.10517714_10517801del | NCBI36 |
NG_028035.1:g.37235_37322del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382483.4:c.329_416del MANE Select | ENSP00000371923.3:p.Pro110GlnfsTer18 | |
ENST00000329335.3:n.579_666del | ||
ENST00000382483.3:c.329_416del | ENSP00000371923.3:p.Pro110GlnfsTer18 | |
NM_178857.5:c.329_416del | NP_849188.4:p.Pro110GlnfsTer18 | |
NM_178857.6:c.329_416del MANE Select | NP_849188.4:p.Pro110GlnfsTer18 |