HGVS | Genome Assembly |
---|---|
NC_000006.12:g.44313329C>T , CM000668.2:g.44313329C>T | GRCh38 |
NC_000006.11:g.44281066C>T , CM000668.1:g.44281066C>T | GRCh37 |
NC_000006.10:g.44389044C>T | NCBI36 |
NG_031952.1:g.4998G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000244571.5:c.-6G>A (AARS2) MANE Select | ENSP00000244571.4:n.-6G>A | |
ENST00000505802.1:c.855+5687C>T | ||
XM_005249245.2:c.-6G>A (AARS2) | XP_005249302.1:n.-6G>A | |
XM_011514764.1:c.-6G>A (AARS2) | XP_011513066.1:n.-6G>A | |
XR_241907.2:n.30G>A (AARS2) | ||
XM_005249245.3:c.-6G>A (AARS2) | XP_005249302.1:n.-6G>A | |
XM_011514764.2:c.-6G>A (AARS2) | XP_011513066.1:n.-6G>A | |
NM_020745.4:c.-6G>A (AARS2) MANE Select | NP_065796.2:n.-6G>A | |
NM_001318876.2:c.946-128561C>T (POLR1C) | NP_001305805.1:n.946-128561C>T |