Canonical Allele Identifier: CA3833927

Linked Data

dbSNP Id: rs771367712
gnomAD v2: 6-44269802-C-T
gnomAD v4: 6-44302065-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44302065C>T , CM000668.2:g.44302065C>T GRCh38
NC_000006.11:g.44269802C>T , CM000668.1:g.44269802C>T GRCh37
NC_000006.10:g.44377780C>T NCBI36
NG_031952.1:g.16262G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000244571.5:c.2593G>A (AARS2) MANE Select ENSP00000244571.4:p.Gly865Arg
ENST00000244571.4:c.2593G>A (AARS2) ENSP00000244571.4:p.Gly865Arg
ENST00000438774.2:c.577-4878C>T (TMEM151B) ENSP00000409337.2:n.577-4878C>T
ENST00000505802.1:c.314-4878C>T
NM_020745.3:c.2593G>A (AARS2) NP_065796.1:p.Gly865Arg
XM_005249245.2:c.2302G>A (AARS2) XP_005249302.1:p.Gly768Arg
XM_011514764.1:c.2593G>A (AARS2) XP_011513066.1:p.Gly865Arg
XR_241907.2:n.2518G>A (AARS2)
XM_005249245.3:c.2302G>A (AARS2) XP_005249302.1:p.Gly768Arg
XM_011514764.2:c.2593G>A (AARS2) XP_011513066.1:p.Gly865Arg
XM_017011112.1:c.1303G>A (AARS2) XP_016866601.1:p.Gly435Arg
NM_020745.4:c.2593G>A (AARS2) MANE Select NP_065796.2:p.Gly865Arg
NM_001318876.2:c.946-139825C>T (POLR1C) NP_001305805.1:n.946-139825C>T