HGVS | Genome Assembly |
---|---|
NC_000002.12:g.232523535_232523536del , CM000664.2:g.232523535_232523536del | GRCh38 |
NC_000002.11:g.233388245_233388246del , CM000664.1:g.233388245_233388246del | GRCh37 |
NC_000002.10:g.233096489_233096490del | NCBI36 |
NG_008028.1:g.2324_2325del | |
NG_031969.1:g.8073_8074del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000617714.2:c.969_970del MANE Select | ENSP00000479745.1:p.Val325GlyfsTer? | |
ENST00000449534.6:c.969_970del | ENSP00000473410.1:p.Val325GlyfsTer? | |
ENST00000617714.1:c.969_970del | ENSP00000479745.1:p.Val325GlyfsTer? | |
NM_001195129.1:c.969_970del | NP_001182058.1:p.Val325GlyfsTer? | |
NM_001195129.2:c.969_970del MANE Select | NP_001182058.1:p.Val325GlyfsTer? | |
NM_001369848.1:c.969_970del | NP_001356777.1:p.Val325GlyfsTer? |