Canonical Allele Identifier: CA3833945

Linked Data

dbSNP Id: rs746361792
gnomAD v2: 6-44269881-C-G
gnomAD v4: 6-44302144-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44302144C>G , CM000668.2:g.44302144C>G GRCh38
NC_000006.11:g.44269881C>G , CM000668.1:g.44269881C>G GRCh37
NC_000006.10:g.44377859C>G NCBI36
NG_031952.1:g.16183G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000244571.5:c.2514G>C (AARS2) MANE Select ENSP00000244571.4:p.Gln838His
ENST00000244571.4:c.2514G>C (AARS2) ENSP00000244571.4:p.Gln838His
ENST00000438774.2:c.577-4799C>G (TMEM151B) ENSP00000409337.2:n.577-4799C>G
ENST00000505802.1:c.314-4799C>G
NM_020745.3:c.2514G>C (AARS2) NP_065796.1:p.Gln838His
XM_005249245.2:c.2223G>C (AARS2) XP_005249302.1:p.Gln741His
XM_011514764.1:c.2514G>C (AARS2) XP_011513066.1:p.Gln838His
XR_241907.2:n.2439G>C (AARS2)
XM_005249245.3:c.2223G>C (AARS2) XP_005249302.1:p.Gln741His
XM_011514764.2:c.2514G>C (AARS2) XP_011513066.1:p.Gln838His
XM_017011112.1:c.1224G>C (AARS2) XP_016866601.1:p.Gln408His
NM_020745.4:c.2514G>C (AARS2) MANE Select NP_065796.2:p.Gln838His
NM_001318876.2:c.946-139746C>G (POLR1C) NP_001305805.1:n.946-139746C>G