Canonical Allele Identifier: CA3833925

Linked Data

dbSNP Id: rs773742164
gnomAD v2: 6-44269799-G-A
gnomAD v4: 6-44302062-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44302062G>A , CM000668.2:g.44302062G>A GRCh38
NC_000006.11:g.44269799G>A , CM000668.1:g.44269799G>A GRCh37
NC_000006.10:g.44377777G>A NCBI36
NG_031952.1:g.16265C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000244571.5:c.2596C>T (AARS2) MANE Select ENSP00000244571.4:p.Gln866Ter
ENST00000244571.4:c.2596C>T (AARS2) ENSP00000244571.4:p.Gln866Ter
ENST00000438774.2:c.577-4881G>A (TMEM151B) ENSP00000409337.2:n.577-4881G>A
ENST00000505802.1:c.314-4881G>A
NM_020745.3:c.2596C>T (AARS2) NP_065796.1:p.Gln866Ter
XM_005249245.2:c.2305C>T (AARS2) XP_005249302.1:p.Gln769Ter
XM_011514764.1:c.2596C>T (AARS2) XP_011513066.1:p.Gln866Ter
XR_241907.2:n.2521C>T (AARS2)
XM_005249245.3:c.2305C>T (AARS2) XP_005249302.1:p.Gln769Ter
XM_011514764.2:c.2596C>T (AARS2) XP_011513066.1:p.Gln866Ter
XM_017011112.1:c.1306C>T (AARS2) XP_016866601.1:p.Gln436Ter
NM_020745.4:c.2596C>T (AARS2) MANE Select NP_065796.2:p.Gln866Ter
NM_001318876.2:c.946-139828G>A (POLR1C) NP_001305805.1:n.946-139828G>A