HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133257074del , CM000671.2:g.133257074del | GRCh38 |
NC_000009.11:g.136132461del , CM000671.1:g.136132461del | GRCh37 |
NC_000009.10:g.135122282del | NCBI36 |
NG_006669.1:g.20594del | |
NG_006669.2:g.23142del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000453660.4:n.403+335del | ||
ENST00000647353.1:n.54-5922del | ||
ENST00000651471.1:n.330-718del | ||
ENST00000679909.1:c.28+18088del | ENSP00000506089.1:n.28+18088del | |
ENST00000453660.3:n.385+335del | ||
ENST00000538324.2:c.371+335del | ENSP00000483018.1:n.371+335del | |
ENST00000611156.4:c.371+335del | ENSP00000483265.1:n.371+335del | |
NM_020469.2:c.374+335del | NP_065202.2:n.374+335del | |
NM_020469.3:c.374+335del | NP_065202.2:n.374+335del |