Canonical Allele Identifier: CA2839935520
Gene: AARS2 HGNC NCBI
POLR1C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44311373G>T , CM000668.2:g.44311373G>T GRCh38
NC_000006.11:g.44279110G>T , CM000668.1:g.44279110G>T GRCh37
NC_000006.10:g.44387088G>T NCBI36
NG_031952.1:g.6954C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000244571.5:c.581+17C>A (AARS2) MANE Select ENSP00000244571.4:n.581+17C>A
ENST00000244571.4:c.581+17C>A (AARS2) ENSP00000244571.4:n.581+17C>A
ENST00000505802.1:c.855+3731G>T
NM_020745.3:c.581+17C>A (AARS2) NP_065796.1:n.581+17C>A
XM_005249245.2:c.581+17C>A (AARS2) XP_005249302.1:n.581+17C>A
XM_011514764.1:c.581+17C>A (AARS2) XP_011513066.1:n.581+17C>A
XR_241907.2:n.616+17C>A (AARS2)
XM_005249245.3:c.581+17C>A (AARS2) XP_005249302.1:n.581+17C>A
XM_011514764.2:c.581+17C>A (AARS2) XP_011513066.1:n.581+17C>A
XM_017011112.1:c.-438+17C>A (AARS2) XP_016866601.1:n.-438+17C>A
NM_020745.4:c.581+17C>A (AARS2) MANE Select NP_065796.2:n.581+17C>A
NM_001318876.2:c.946-130517G>T (POLR1C) NP_001305805.1:n.946-130517G>T