HGVS | Genome Assembly |
---|---|
NC_000006.12:g.44313343T>A , CM000668.2:g.44313343T>A | GRCh38 |
NC_000006.11:g.44281080T>A , CM000668.1:g.44281080T>A | GRCh37 |
NC_000006.10:g.44389058T>A | NCBI36 |
NG_031952.1:g.4984A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000244571.5:c.-20A>T (AARS2) MANE Select | ENSP00000244571.4:n.-20A>T | |
ENST00000505802.1:c.855+5701T>A | ||
XM_005249245.2:c.-20A>T (AARS2) | XP_005249302.1:n.-20A>T | |
XM_011514764.1:c.-20A>T (AARS2) | XP_011513066.1:n.-20A>T | |
XR_241907.2:n.16A>T (AARS2) | ||
XM_005249245.3:c.-20A>T (AARS2) | XP_005249302.1:n.-20A>T | |
XM_011514764.2:c.-20A>T (AARS2) | XP_011513066.1:n.-20A>T | |
NM_020745.4:c.-20A>T (AARS2) MANE Select | NP_065796.2:n.-20A>T | |
NM_001318876.2:c.946-128547T>A (POLR1C) | NP_001305805.1:n.946-128547T>A |