Canonical Allele Identifier: CA1624928794
Gene: AARS2 HGNC NCBI
POLR1C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44311098A= , CM000668.2:g.44311098A= GRCh38
NC_000006.11:g.44278835A= , CM000668.1:g.44278835A= GRCh37
NC_000006.10:g.44386813A= NCBI36
NG_031952.1:g.7229T=

Transcript Alleles

HGVS Amino-acid change
ENST00000244571.5:c.645T= (AARS2) MANE Select ENSP00000244571.4:p.Thr215=
ENST00000244571.4:c.645T= (AARS2) ENSP00000244571.4:p.Thr215=
ENST00000505802.1:c.855+3456A=
NM_020745.3:c.645T= (AARS2) NP_065796.1:p.Thr215=
XM_005249245.2:c.645T= (AARS2) XP_005249302.1:p.Thr215=
XM_011514764.1:c.645T= (AARS2) XP_011513066.1:p.Thr215=
XR_241907.2:n.680T= (AARS2)
XM_005249245.3:c.645T= (AARS2) XP_005249302.1:p.Thr215=
XM_011514764.2:c.645T= (AARS2) XP_011513066.1:p.Thr215=
XM_017011112.1:c.-374T= (AARS2) XP_016866601.1:n.-374T=
NM_020745.4:c.645T= (AARS2) MANE Select NP_065796.2:p.Thr215=
NM_001318876.2:c.946-130792A= (POLR1C) NP_001305805.1:n.946-130792A=