HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133257330del , CM000671.2:g.133257330del | GRCh38 |
NC_000009.11:g.136132717del , CM000671.1:g.136132717del | GRCh37 |
NC_000009.10:g.135122538del | NCBI36 |
NG_006669.1:g.20338del | |
NG_006669.2:g.22886del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000453660.4:n.403+79del | ||
ENST00000647353.1:n.54-6178del | ||
ENST00000651471.1:n.329+712del | ||
ENST00000679909.1:c.28+17832del | ENSP00000506089.1:n.28+17832del | |
ENST00000453660.3:n.385+79del | ||
ENST00000538324.2:c.371+79del | ENSP00000483018.1:n.371+79del | |
ENST00000611156.4:c.371+79del | ENSP00000483265.1:n.371+79del | |
NM_020469.2:c.374+79del | NP_065202.2:n.374+79del | |
NM_020469.3:c.374+79del | NP_065202.2:n.374+79del |