Canonical Allele Identifier: CA3834106

Linked Data

dbSNP Id: rs374971594
gnomAD v2: 6-44271063-G-C
gnomAD v4: 6-44303326-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44303326G>C , CM000668.2:g.44303326G>C GRCh38
NC_000006.11:g.44271063G>C , CM000668.1:g.44271063G>C GRCh37
NC_000006.10:g.44379041G>C NCBI36
NG_031952.1:g.15001C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000244571.5:c.2105C>G (AARS2) MANE Select ENSP00000244571.4:p.Ala702Gly
ENST00000244571.4:c.2105C>G (AARS2) ENSP00000244571.4:p.Ala702Gly
ENST00000438774.2:c.577-3617G>C (TMEM151B) ENSP00000409337.2:n.577-3617G>C
ENST00000505802.1:c.314-3617G>C
NM_020745.3:c.2105C>G (AARS2) NP_065796.1:p.Ala702Gly
XM_005249245.2:c.1814C>G (AARS2) XP_005249302.1:p.Ala605Gly
XM_011514764.1:c.2105C>G (AARS2) XP_011513066.1:p.Ala702Gly
XR_241907.2:n.2140C>G (AARS2)
XM_005249245.3:c.1814C>G (AARS2) XP_005249302.1:p.Ala605Gly
XM_011514764.2:c.2105C>G (AARS2) XP_011513066.1:p.Ala702Gly
XM_017011112.1:c.815C>G (AARS2) XP_016866601.1:p.Ala272Gly
NM_020745.4:c.2105C>G (AARS2) MANE Select NP_065796.2:p.Ala702Gly
NM_001318876.2:c.946-138564G>C (POLR1C) NP_001305805.1:n.946-138564G>C