Canonical Allele Identifier: CA138396121
Gene: AARS2 HGNC NCBI
POLR1C HGNC NCBI

Linked Data

dbSNP Id: rs930548116
gnomAD v4: 6-44313235-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44313235A>G , CM000668.2:g.44313235A>G GRCh38
NC_000006.11:g.44280972A>G , CM000668.1:g.44280972A>G GRCh37
NC_000006.10:g.44388950A>G NCBI36
NG_031952.1:g.5092T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000244571.5:c.89T>C (AARS2) MANE Select ENSP00000244571.4:p.Leu30Pro
ENST00000244571.4:c.89T>C (AARS2) ENSP00000244571.4:p.Leu30Pro
ENST00000505802.1:c.855+5593A>G
NM_020745.3:c.89T>C (AARS2) NP_065796.1:p.Leu30Pro
XM_005249245.2:c.89T>C (AARS2) XP_005249302.1:p.Leu30Pro
XM_011514764.1:c.89T>C (AARS2) XP_011513066.1:p.Leu30Pro
XR_241907.2:n.124T>C (AARS2)
XM_005249245.3:c.89T>C (AARS2) XP_005249302.1:p.Leu30Pro
XM_011514764.2:c.89T>C (AARS2) XP_011513066.1:p.Leu30Pro
NM_020745.4:c.89T>C (AARS2) MANE Select NP_065796.2:p.Leu30Pro
NM_001318876.2:c.946-128655A>G (POLR1C) NP_001305805.1:n.946-128655A>G