HGVS | Genome Assembly |
---|---|
NC_000002.12:g.29071044_29071046del , CM000664.2:g.29071044_29071046del | GRCh38 |
NC_000002.11:g.29293910_29293912del , CM000664.1:g.29293910_29293912del | GRCh37 |
NC_000002.10:g.29147414_29147416del | NCBI36 |
NG_021427.1:g.8219_8221del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331664.6:c.3219_3221del MANE Select | ENSP00000332809.4:p.Pro1074del | |
ENST00000331664.5:c.3219_3221del | ENSP00000332809.4:p.Pro1074del | |
NM_001029883.2:c.3219_3221del | NP_001025054.1:p.Pro1074del | |
XM_011532826.1:c.3219_3221del | XP_011531128.1:p.Pro1074del | |
XR_939901.1:n.185+1877_185+1879del | ||
XR_939902.1:n.173+1889_173+1891del | ||
NM_001029883.3:c.3219_3221del MANE Select | NP_001025054.1:p.Pro1074del |