Canonical Allele Identifier: CA3834059

Linked Data

dbSNP Id: rs370007720
gnomAD v2: 6-44270810-A-G
gnomAD v3: 6-44303073-A-G
gnomAD v4: 6-44303073-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44303073A>G , CM000668.2:g.44303073A>G GRCh38
NC_000006.11:g.44270810A>G , CM000668.1:g.44270810A>G GRCh37
NC_000006.10:g.44378788A>G NCBI36
NG_031952.1:g.15254T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000244571.5:c.2248T>C (AARS2) MANE Select ENSP00000244571.4:p.Cys750Arg
ENST00000244571.4:c.2248T>C (AARS2) ENSP00000244571.4:p.Cys750Arg
ENST00000438774.2:c.577-3870A>G (TMEM151B) ENSP00000409337.2:n.577-3870A>G
ENST00000505802.1:c.314-3870A>G
NM_020745.3:c.2248T>C (AARS2) NP_065796.1:p.Cys750Arg
XM_005249245.2:c.1957T>C (AARS2) XP_005249302.1:p.Cys653Arg
XM_011514764.1:c.2248T>C (AARS2) XP_011513066.1:p.Cys750Arg
XR_241907.2:n.2181-163T>C (AARS2)
XM_005249245.3:c.1957T>C (AARS2) XP_005249302.1:p.Cys653Arg
XM_011514764.2:c.2248T>C (AARS2) XP_011513066.1:p.Cys750Arg
XM_017011112.1:c.958T>C (AARS2) XP_016866601.1:p.Cys320Arg
NM_020745.4:c.2248T>C (AARS2) MANE Select NP_065796.2:p.Cys750Arg
NM_001318876.2:c.946-138817A>G (POLR1C) NP_001305805.1:n.946-138817A>G