HGVS | Genome Assembly |
---|---|
NC_000012.12:g.57739591C>A , CM000674.2:g.57739591C>A | GRCh38 |
NC_000012.11:g.58133374C>A , CM000674.1:g.58133374C>A | GRCh37 |
NC_000012.10:g.56419641C>A | NCBI36 |
NG_029755.1:g.7571G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000257897.7:c.160+2321G>T (AGAP2) | ENSP00000257897.3:n.160+2321G>T | |
ENST00000553221.5:n.189+1390C>A (TSPAN31) | ||
NM_014770.3:c.160+2321G>T (AGAP2) | NP_055585.1:n.160+2321G>T | |
XM_005268626.1:c.160+2321G>T (AGAP2) | XP_005268683.1:n.160+2321G>T | |
XM_005268626.2:c.160+2321G>T (AGAP2) | XP_005268683.1:n.160+2321G>T | |
NM_014770.4:c.160+2321G>T (AGAP2) | NP_055585.1:n.160+2321G>T |