HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133262080A= , CM000671.2:g.133262080A= | GRCh38 |
NC_000009.11:g.136137483A= , CM000671.1:g.136137483A= | GRCh37 |
NC_000009.10:g.135127304A= | NCBI36 |
NG_006669.1:g.15569T= | |
NG_006669.2:g.18135T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000453660.4:n.128+19T= | ||
ENST00000647353.1:n.54-10928T= | ||
ENST00000651471.1:n.133+19T= | ||
ENST00000679909.1:c.28+13082T= | ENSP00000506089.1:n.28+13082T= | |
ENST00000453660.3:n.110+19T= | ||
ENST00000538324.2:c.98+19T= | ENSP00000483018.1:n.98+19T= | |
ENST00000611156.4:c.98+19T= | ENSP00000483265.1:n.98+19T= | |
NM_020469.2:c.98+19T= | NP_065202.2:n.98+19T= | |
NM_020469.3:c.98+19T= | NP_065202.2:n.98+19T= |