Canonical Allele Identifier: CA1624928744
Gene: AARS2 HGNC NCBI
POLR1C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44311070G= , CM000668.2:g.44311070G= GRCh38
NC_000006.11:g.44278807G= , CM000668.1:g.44278807G= GRCh37
NC_000006.10:g.44386785G= NCBI36
NG_031952.1:g.7257C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000244571.5:c.673C= (AARS2) MANE Select ENSP00000244571.4:p.His225=
ENST00000244571.4:c.673C= (AARS2) ENSP00000244571.4:p.His225=
ENST00000505802.1:c.855+3428G=
NM_020745.3:c.673C= (AARS2) NP_065796.1:p.His225=
XM_005249245.2:c.673C= (AARS2) XP_005249302.1:p.His225=
XM_011514764.1:c.673C= (AARS2) XP_011513066.1:p.His225=
XR_241907.2:n.708C= (AARS2)
XM_005249245.3:c.673C= (AARS2) XP_005249302.1:p.His225=
XM_011514764.2:c.673C= (AARS2) XP_011513066.1:p.His225=
XM_017011112.1:c.-346C= (AARS2) XP_016866601.1:n.-346C=
NM_020745.4:c.673C= (AARS2) MANE Select NP_065796.2:p.His225=
NM_001318876.2:c.946-130820G= (POLR1C) NP_001305805.1:n.946-130820G=