Canonical Allele Identifier: CA3834060

Linked Data

dbSNP Id: rs751129588
gnomAD v2: 6-44270811-G-A
gnomAD v4: 6-44303074-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44303074G>A , CM000668.2:g.44303074G>A GRCh38
NC_000006.11:g.44270811G>A , CM000668.1:g.44270811G>A GRCh37
NC_000006.10:g.44378789G>A NCBI36
NG_031952.1:g.15253C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000244571.5:c.2247C>T (AARS2) MANE Select ENSP00000244571.4:p.Cys749=
ENST00000244571.4:c.2247C>T (AARS2) ENSP00000244571.4:p.Cys749=
ENST00000438774.2:c.577-3869G>A (TMEM151B) ENSP00000409337.2:n.577-3869G>A
ENST00000505802.1:c.314-3869G>A
NM_020745.3:c.2247C>T (AARS2) NP_065796.1:p.Cys749=
XM_005249245.2:c.1956C>T (AARS2) XP_005249302.1:p.Cys652=
XM_011514764.1:c.2247C>T (AARS2) XP_011513066.1:p.Cys749=
XR_241907.2:n.2181-164C>T (AARS2)
XM_005249245.3:c.1956C>T (AARS2) XP_005249302.1:p.Cys652=
XM_011514764.2:c.2247C>T (AARS2) XP_011513066.1:p.Cys749=
XM_017011112.1:c.957C>T (AARS2) XP_016866601.1:p.Cys319=
NM_020745.4:c.2247C>T (AARS2) MANE Select NP_065796.2:p.Cys749=
NM_001318876.2:c.946-138816G>A (POLR1C) NP_001305805.1:n.946-138816G>A