HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154903976del , CM000685.2:g.154903976del | GRCh38 |
NC_000023.10:g.154132251del , CM000685.1:g.154132251del | GRCh37 |
NC_000023.9:g.153785445del | NCBI36 |
NG_011403.1:g.123750del | |
NG_011403.2:g.123750del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.5930del MANE Select | ENSP00000353393.4:p.Phe1977SerfsTer? | |
ENST00000360256.8:c.5930del | ENSP00000353393.4:p.Phe1977SerfsTer? | |
NM_000132.3:c.5930del | NP_000123.1:p.Phe1977SerfsTer? | |
XM_011531126.1:c.5825del | XP_011529428.1:p.Phe1942SerfsTer? | |
NM_000132.4:c.5930del MANE Select | NP_000123.1:p.Phe1977SerfsTer? |