Canonical Allele Identifier: CA450315455

Linked Data

gnomAD v4: 6-44300619-T-C
MyVariant Identifiers: chr6:g.44268356T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44300619T>C , CM000668.2:g.44300619T>C GRCh38
NC_000006.11:g.44268356T>C , CM000668.1:g.44268356T>C GRCh37
NC_000006.10:g.44376334T>C NCBI36
NG_031952.1:g.17708A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000244571.5:c.2886A>G (AARS2) MANE Select ENSP00000244571.4:p.Gln962=
ENST00000244571.4:c.2886A>G (AARS2) ENSP00000244571.4:p.Gln962=
ENST00000438774.2:c.577-6324T>C (TMEM151B) ENSP00000409337.2:n.577-6324T>C
ENST00000491573.1:n.688A>G (AARS2)
ENST00000505802.1:c.314-6324T>C
NM_020745.3:c.2886A>G (AARS2) NP_065796.1:p.Gln962=
XM_005249245.2:c.2595A>G (AARS2) XP_005249302.1:p.Gln865=
XM_011514764.1:c.2793+537A>G (AARS2) XP_011513066.1:n.2793+537A>G
XR_241907.2:n.2811A>G (AARS2)
XM_005249245.3:c.2595A>G (AARS2) XP_005249302.1:p.Gln865=
XM_011514764.2:c.2793+537A>G (AARS2) XP_011513066.1:n.2793+537A>G
XM_017011112.1:c.1596A>G (AARS2) XP_016866601.1:p.Gln532=
NM_020745.4:c.2886A>G (AARS2) MANE Select NP_065796.2:p.Gln962=
NM_001318876.2:c.946-141271T>C (POLR1C) NP_001305805.1:n.946-141271T>C