HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133257060G= , CM000671.2:g.133257060G= | GRCh38 |
NC_000009.11:g.136132447G= , CM000671.1:g.136132447G= | GRCh37 |
NC_000009.10:g.135122268G= | NCBI36 |
NG_006669.1:g.20608C= | |
NG_006669.2:g.23156C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000453660.4:n.403+349C= | ||
ENST00000647353.1:n.54-5908C= | ||
ENST00000651471.1:n.330-704C= | ||
ENST00000679909.1:c.28+18102C= | ENSP00000506089.1:n.28+18102C= | |
ENST00000453660.3:n.385+349C= | ||
ENST00000538324.2:c.371+349C= | ENSP00000483018.1:n.371+349C= | |
ENST00000611156.4:c.371+349C= | ENSP00000483265.1:n.371+349C= | |
NM_020469.2:c.374+349C= | NP_065202.2:n.374+349C= | |
NM_020469.3:c.374+349C= | NP_065202.2:n.374+349C= |