HGVS | Genome Assembly |
---|---|
NC_000012.12:g.65170067_65170069del , CM000674.2:g.65170067_65170069del | GRCh38 |
NC_000012.11:g.65563847_65563849del , CM000674.1:g.65563847_65563849del | GRCh37 |
NC_000012.10:g.63850114_63850116del | NCBI36 |
NG_016210.1:g.5497_5499del | |
NG_016210.2:g.5497_5499del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308330.3:c.471_473del MANE Select | ENSP00000308369.2:p.Gly158del | |
ENST00000308330.2:c.471_473del | ENSP00000308369.2:p.Gly158del | |
ENST00000541171.1:n.485_487del | ||
NM_001167614.1:c.471_473del | NP_001161086.1:p.Gly158del | |
NM_014319.4:c.471_473del | NP_055134.2:p.Gly158del | |
NM_014319.5:c.471_473del MANE Select | NP_055134.2:p.Gly158del | |
NM_001167614.2:c.471_473del | NP_001161086.1:p.Gly158del |