HGVS | Genome Assembly |
---|---|
NC_000012.12:g.57739524A= , CM000674.2:g.57739524A= | GRCh38 |
NC_000012.11:g.58133307A= , CM000674.1:g.58133307A= | GRCh37 |
NC_000012.10:g.56419574A= | NCBI36 |
NG_029755.1:g.7638T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000257897.7:c.160+2388T= (AGAP2) | ENSP00000257897.3:n.160+2388T= | |
ENST00000553221.5:n.189+1323A= (TSPAN31) | ||
NM_014770.3:c.160+2388T= (AGAP2) | NP_055585.1:n.160+2388T= | |
XM_005268626.1:c.160+2388T= (AGAP2) | XP_005268683.1:n.160+2388T= | |
XM_005268626.2:c.160+2388T= (AGAP2) | XP_005268683.1:n.160+2388T= | |
NM_014770.4:c.160+2388T= (AGAP2) | NP_055585.1:n.160+2388T= |