HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133255607A= , CM000671.2:g.133255607A= | GRCh38 |
NC_000009.11:g.136130994A= , CM000671.1:g.136130994A= | GRCh37 |
NC_000009.10:g.135120815A= | NCBI36 |
NG_006669.1:g.22061T= | |
NG_006669.2:g.24609T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000453660.4:n.1153T= | ||
ENST00000647353.1:n.54-4455T= | ||
ENST00000679909.1:c.28+19555T= | ENSP00000506089.1:n.28+19555T= | |
ENST00000453660.3:n.1135T= | ||
ENST00000538324.2:c.1117T= | ENSP00000483018.1:p.Phe373= | |
ENST00000611156.4:c.*59T= | ENSP00000483265.1:n.*59T= | |
NM_020469.2:c.*59T= | NP_065202.2:n.*59T= | |
NM_020469.3:c.*59T= | NP_065202.2:n.*59T= |