Canonical Allele Identifier: CA450391960
Gene: AARS2 HGNC NCBI
POLR1C HGNC NCBI

Linked Data

gnomAD v4: 6-44313261-T-A
MyVariant Identifiers: chr6:g.44280998T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44313261T>A , CM000668.2:g.44313261T>A GRCh38
NC_000006.11:g.44280998T>A , CM000668.1:g.44280998T>A GRCh37
NC_000006.10:g.44388976T>A NCBI36
NG_031952.1:g.5066A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000244571.5:c.63A>T (AARS2) MANE Select ENSP00000244571.4:p.Ala21=
ENST00000244571.4:c.63A>T (AARS2) ENSP00000244571.4:p.Ala21=
ENST00000505802.1:c.855+5619T>A
NM_020745.3:c.63A>T (AARS2) NP_065796.1:p.Ala21=
XM_005249245.2:c.63A>T (AARS2) XP_005249302.1:p.Ala21=
XM_011514764.1:c.63A>T (AARS2) XP_011513066.1:p.Ala21=
XR_241907.2:n.98A>T (AARS2)
XM_005249245.3:c.63A>T (AARS2) XP_005249302.1:p.Ala21=
XM_011514764.2:c.63A>T (AARS2) XP_011513066.1:p.Ala21=
NM_020745.4:c.63A>T (AARS2) MANE Select NP_065796.2:p.Ala21=
NM_001318876.2:c.946-128629T>A (POLR1C) NP_001305805.1:n.946-128629T>A