Canonical Allele Identifier: CA138396173
Gene: AARS2 HGNC NCBI
POLR1C HGNC NCBI

Linked Data

dbSNP Id: rs1049916671
gnomAD v2: 6-44281004-C-T
gnomAD v4: 6-44313267-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44313267C>T , CM000668.2:g.44313267C>T GRCh38
NC_000006.11:g.44281004C>T , CM000668.1:g.44281004C>T GRCh37
NC_000006.10:g.44388982C>T NCBI36
NG_031952.1:g.5060G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000244571.5:c.57G>A (AARS2) MANE Select ENSP00000244571.4:p.Ser19=
ENST00000244571.4:c.57G>A (AARS2) ENSP00000244571.4:p.Ser19=
ENST00000505802.1:c.855+5625C>T
NM_020745.3:c.57G>A (AARS2) NP_065796.1:p.Ser19=
XM_005249245.2:c.57G>A (AARS2) XP_005249302.1:p.Ser19=
XM_011514764.1:c.57G>A (AARS2) XP_011513066.1:p.Ser19=
XR_241907.2:n.92G>A (AARS2)
XM_005249245.3:c.57G>A (AARS2) XP_005249302.1:p.Ser19=
XM_011514764.2:c.57G>A (AARS2) XP_011513066.1:p.Ser19=
NM_020745.4:c.57G>A (AARS2) MANE Select NP_065796.2:p.Ser19=
NM_001318876.2:c.946-128623C>T (POLR1C) NP_001305805.1:n.946-128623C>T