Canonical Allele Identifier: CA450391934
Gene: AARS2 HGNC NCBI
POLR1C HGNC NCBI

Linked Data

gnomAD v4: 6-44313228-C-T
MyVariant Identifiers: chr6:g.44280965C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44313228C>T , CM000668.2:g.44313228C>T GRCh38
NC_000006.11:g.44280965C>T , CM000668.1:g.44280965C>T GRCh37
NC_000006.10:g.44388943C>T NCBI36
NG_031952.1:g.5099G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000244571.5:c.96G>A (AARS2) MANE Select ENSP00000244571.4:p.Ser32=
ENST00000244571.4:c.96G>A (AARS2) ENSP00000244571.4:p.Ser32=
ENST00000505802.1:c.855+5586C>T
NM_020745.3:c.96G>A (AARS2) NP_065796.1:p.Ser32=
XM_005249245.2:c.96G>A (AARS2) XP_005249302.1:p.Ser32=
XM_011514764.1:c.96G>A (AARS2) XP_011513066.1:p.Ser32=
XR_241907.2:n.131G>A (AARS2)
XM_005249245.3:c.96G>A (AARS2) XP_005249302.1:p.Ser32=
XM_011514764.2:c.96G>A (AARS2) XP_011513066.1:p.Ser32=
NM_020745.4:c.96G>A (AARS2) MANE Select NP_065796.2:p.Ser32=
NM_001318876.2:c.946-128662C>T (POLR1C) NP_001305805.1:n.946-128662C>T