Canonical Allele Identifier: CA138386114

Gene: AARS2 TMEM151B POLR1C

Linked Data

• dbSNP Id: rs913947204
• gnomAD v2: 6-44271089-A-T
• MyVariant Identifiers: chr6:g.44271089A>T (hg19) ; chr6:g.44303352A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44303352A>T , CM000668.2:g.44303352A>T	GRCh38
NC_000006.11:g.44271089A>T , CM000668.1:g.44271089A>T	GRCh37
NC_000006.10:g.44379067A>T	NCBI36
NG_031952.1:g.14975T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244571.5:c.2079T>A (AARS2) MANE Select	ENSP00000244571.4:p.Ala693=
ENST00000244571.4:c.2079T>A (AARS2)	ENSP00000244571.4:p.Ala693=
ENST00000438774.2:c.577-3591A>T (TMEM151B)	ENSP00000409337.2:n.577-3591A>T
ENST00000505802.1:c.314-3591A>T
NM_020745.3:c.2079T>A (AARS2)	NP_065796.1:p.Ala693=
XM_005249245.2:c.1788T>A (AARS2)	XP_005249302.1:p.Ala596=
XM_011514764.1:c.2079T>A (AARS2)	XP_011513066.1:p.Ala693=
XR_241907.2:n.2114T>A (AARS2)
XM_005249245.3:c.1788T>A (AARS2)	XP_005249302.1:p.Ala596=
XM_011514764.2:c.2079T>A (AARS2)	XP_011513066.1:p.Ala693=
XM_017011112.1:c.789T>A (AARS2)	XP_016866601.1:p.Ala263=
NM_020745.4:c.2079T>A (AARS2) MANE Select	NP_065796.2:p.Ala693=
NM_001318876.2:c.946-138538A>T (POLR1C)	NP_001305805.1:n.946-138538A>T