Canonical Allele Identifier: CA450315442

Gene: AARS2 TMEM151B POLR1C

Linked Data

• MyVariant Identifiers: chr6:g.44268338A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44300601A>T , CM000668.2:g.44300601A>T	GRCh38
NC_000006.11:g.44268338A>T , CM000668.1:g.44268338A>T	GRCh37
NC_000006.10:g.44376316A>T	NCBI36
NG_031952.1:g.17726T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244571.5:c.2904T>A (AARS2) MANE Select	ENSP00000244571.4:p.Thr968=
ENST00000244571.4:c.2904T>A (AARS2)	ENSP00000244571.4:p.Thr968=
ENST00000438774.2:c.577-6342A>T (TMEM151B)	ENSP00000409337.2:n.577-6342A>T
ENST00000491573.1:n.706T>A (AARS2)
ENST00000505802.1:c.314-6342A>T
NM_020745.3:c.2904T>A (AARS2)	NP_065796.1:p.Thr968=
XM_005249245.2:c.2613T>A (AARS2)	XP_005249302.1:p.Thr871=
XM_011514764.1:c.2793+555T>A (AARS2)	XP_011513066.1:n.2793+555T>A
XR_241907.2:n.2829T>A (AARS2)
XM_005249245.3:c.2613T>A (AARS2)	XP_005249302.1:p.Thr871=
XM_011514764.2:c.2793+555T>A (AARS2)	XP_011513066.1:n.2793+555T>A
XM_017011112.1:c.1614T>A (AARS2)	XP_016866601.1:p.Thr538=
NM_020745.4:c.2904T>A (AARS2) MANE Select	NP_065796.2:p.Thr968=
NM_001318876.2:c.946-141289A>T (POLR1C)	NP_001305805.1:n.946-141289A>T