Canonical Allele Identifier: CA364336418

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44302070T>C , CM000668.2:g.44302070T>C GRCh38
NC_000006.11:g.44269807T>C , CM000668.1:g.44269807T>C GRCh37
NC_000006.10:g.44377785T>C NCBI36
NG_031952.1:g.16257A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000244571.5:c.2588A>G (AARS2) MANE Select ENSP00000244571.4:p.Gln863Arg
ENST00000244571.4:c.2588A>G (AARS2) ENSP00000244571.4:p.Gln863Arg
ENST00000438774.2:c.577-4873T>C (TMEM151B) ENSP00000409337.2:n.577-4873T>C
ENST00000505802.1:c.314-4873T>C
NM_020745.3:c.2588A>G (AARS2) NP_065796.1:p.Gln863Arg
XM_005249245.2:c.2297A>G (AARS2) XP_005249302.1:p.Gln766Arg
XM_011514764.1:c.2588A>G (AARS2) XP_011513066.1:p.Gln863Arg
XR_241907.2:n.2513A>G (AARS2)
XM_005249245.3:c.2297A>G (AARS2) XP_005249302.1:p.Gln766Arg
XM_011514764.2:c.2588A>G (AARS2) XP_011513066.1:p.Gln863Arg
XM_017011112.1:c.1298A>G (AARS2) XP_016866601.1:p.Gln433Arg
NM_020745.4:c.2588A>G (AARS2) MANE Select NP_065796.2:p.Gln863Arg
NM_001318876.2:c.946-139820T>C (POLR1C) NP_001305805.1:n.946-139820T>C