HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133261771C= , CM000671.2:g.133261771C= | GRCh38 |
NC_000009.11:g.136137174C= , CM000671.1:g.136137174C= | GRCh37 |
NC_000009.10:g.135126995C= | NCBI36 |
NG_006669.1:g.15879G= | |
NG_006669.2:g.18444G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000453660.4:n.128+328G= | ||
ENST00000647353.1:n.54-10619G= | ||
ENST00000651471.1:n.133+328G= | ||
ENST00000679909.1:c.28+13391G= | ENSP00000506089.1:n.28+13391G= | |
ENST00000453660.3:n.110+328G= | ||
ENST00000538324.2:c.98+328G= | ENSP00000483018.1:n.98+328G= | |
ENST00000611156.4:c.98+328G= | ENSP00000483265.1:n.98+328G= | |
NM_020469.2:c.98+328G= | NP_065202.2:n.98+328G= | |
NM_020469.3:c.98+328G= | NP_065202.2:n.98+328G= |