HGVS | Genome Assembly |
---|---|
NC_000006.12:g.44313345T= , CM000668.2:g.44313345T= | GRCh38 |
NC_000006.11:g.44281082T= , CM000668.1:g.44281082T= | GRCh37 |
NC_000006.10:g.44389060T= | NCBI36 |
NG_031952.1:g.4982A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000244571.5:c.-22A= (AARS2) MANE Select | ENSP00000244571.4:n.-22A= | |
ENST00000505802.1:c.855+5703T= | ||
XM_005249245.2:c.-22A= (AARS2) | XP_005249302.1:n.-22A= | |
XM_011514764.1:c.-22A= (AARS2) | XP_011513066.1:n.-22A= | |
XR_241907.2:n.14A= (AARS2) | ||
XM_005249245.3:c.-22A= (AARS2) | XP_005249302.1:n.-22A= | |
XM_011514764.2:c.-22A= (AARS2) | XP_011513066.1:n.-22A= | |
NM_020745.4:c.-22A= (AARS2) MANE Select | NP_065796.2:n.-22A= | |
NM_001318876.2:c.946-128545T= (POLR1C) | NP_001305805.1:n.946-128545T= |