HGVS | Genome Assembly |
---|---|
NC_000012.12:g.57739436A>T , CM000674.2:g.57739436A>T | GRCh38 |
NC_000012.11:g.58133219A>T , CM000674.1:g.58133219A>T | GRCh37 |
NC_000012.10:g.56419486A>T | NCBI36 |
NG_029755.1:g.7726T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000257897.7:c.160+2476T>A (AGAP2) | ENSP00000257897.3:n.160+2476T>A | |
ENST00000553221.5:n.189+1235A>T (TSPAN31) | ||
NM_014770.3:c.160+2476T>A (AGAP2) | NP_055585.1:n.160+2476T>A | |
XM_005268626.1:c.160+2476T>A (AGAP2) | XP_005268683.1:n.160+2476T>A | |
XM_005268626.2:c.160+2476T>A (AGAP2) | XP_005268683.1:n.160+2476T>A | |
NM_014770.4:c.160+2476T>A (AGAP2) | NP_055585.1:n.160+2476T>A |