Canonical Allele Identifier: CA450391323
Gene: AARS2 HGNC NCBI
POLR1C HGNC NCBI

Linked Data

dbSNP Id: rs1786303816
MyVariant Identifiers: chr6:g.44278766T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44311029T>G , CM000668.2:g.44311029T>G GRCh38
NC_000006.11:g.44278766T>G , CM000668.1:g.44278766T>G GRCh37
NC_000006.10:g.44386744T>G NCBI36
NG_031952.1:g.7298A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000244571.5:c.714A>C (AARS2) MANE Select ENSP00000244571.4:p.Val238=
ENST00000244571.4:c.714A>C (AARS2) ENSP00000244571.4:p.Val238=
ENST00000505802.1:c.855+3387T>G
NM_020745.3:c.714A>C (AARS2) NP_065796.1:p.Val238=
XM_005249245.2:c.714A>C (AARS2) XP_005249302.1:p.Val238=
XM_011514764.1:c.714A>C (AARS2) XP_011513066.1:p.Val238=
XR_241907.2:n.749A>C (AARS2)
XM_005249245.3:c.714A>C (AARS2) XP_005249302.1:p.Val238=
XM_011514764.2:c.714A>C (AARS2) XP_011513066.1:p.Val238=
XM_017011112.1:c.-305A>C (AARS2) XP_016866601.1:n.-305A>C
NM_020745.4:c.714A>C (AARS2) MANE Select NP_065796.2:p.Val238=
NM_001318876.2:c.946-130861T>G (POLR1C) NP_001305805.1:n.946-130861T>G