Canonical Allele Identifier: CA364342270
Gene: AARS2 HGNC NCBI
POLR1C HGNC NCBI

Linked Data

dbSNP Id: rs1357054107
gnomAD v2: 6-44281006-A-G
gnomAD v4: 6-44313269-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44313269A>G , CM000668.2:g.44313269A>G GRCh38
NC_000006.11:g.44281006A>G , CM000668.1:g.44281006A>G GRCh37
NC_000006.10:g.44388984A>G NCBI36
NG_031952.1:g.5058T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000244571.5:c.55T>C (AARS2) MANE Select ENSP00000244571.4:p.Ser19Pro
ENST00000244571.4:c.55T>C (AARS2) ENSP00000244571.4:p.Ser19Pro
ENST00000505802.1:c.855+5627A>G
NM_020745.3:c.55T>C (AARS2) NP_065796.1:p.Ser19Pro
XM_005249245.2:c.55T>C (AARS2) XP_005249302.1:p.Ser19Pro
XM_011514764.1:c.55T>C (AARS2) XP_011513066.1:p.Ser19Pro
XR_241907.2:n.90T>C (AARS2)
XM_005249245.3:c.55T>C (AARS2) XP_005249302.1:p.Ser19Pro
XM_011514764.2:c.55T>C (AARS2) XP_011513066.1:p.Ser19Pro
NM_020745.4:c.55T>C (AARS2) MANE Select NP_065796.2:p.Ser19Pro
NM_001318876.2:c.946-128621A>G (POLR1C) NP_001305805.1:n.946-128621A>G