HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240868811T>A , CM000664.2:g.240868811T>A | GRCh38 |
NC_000002.11:g.241808228T>A , CM000664.1:g.241808228T>A | GRCh37 |
NC_000002.10:g.241456901T>A | NCBI36 |
NG_008005.1:g.5067T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000307503.3:c.-55T>A | ENSP00000302620.3:n.-55T>A | |
NM_000030.2:c.-55T>A | NP_000021.1:n.-55T>A | |
XR_924060.1:n.405+1422A>T |