Canonical Allele Identifier: CA3834760
Gene: AARS2 HGNC NCBI
POLR1C HGNC NCBI

Linked Data

ClinVar Variation Id: 1314020
dbSNP Id: rs537231845
gnomAD v2: 6-44281036-C-A
gnomAD v3: 6-44313299-C-A
gnomAD v4: 6-44313299-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44313299C>A , CM000668.2:g.44313299C>A GRCh38
NC_000006.11:g.44281036C>A , CM000668.1:g.44281036C>A GRCh37
NC_000006.10:g.44389014C>A NCBI36
NG_031952.1:g.5028G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000244571.5:c.25G>T (AARS2) MANE Select ENSP00000244571.4:p.Ala9Ser
ENST00000244571.4:c.25G>T (AARS2) ENSP00000244571.4:p.Ala9Ser
ENST00000505802.1:c.855+5657C>A
NM_020745.3:c.25G>T (AARS2) NP_065796.1:p.Ala9Ser
XM_005249245.2:c.25G>T (AARS2) XP_005249302.1:p.Ala9Ser
XM_011514764.1:c.25G>T (AARS2) XP_011513066.1:p.Ala9Ser
XR_241907.2:n.60G>T (AARS2)
XM_005249245.3:c.25G>T (AARS2) XP_005249302.1:p.Ala9Ser
XM_011514764.2:c.25G>T (AARS2) XP_011513066.1:p.Ala9Ser
NM_020745.4:c.25G>T (AARS2) MANE Select NP_065796.2:p.Ala9Ser
NM_001318876.2:c.946-128591C>A (POLR1C) NP_001305805.1:n.946-128591C>A