Canonical Allele Identifier: CA364337567

Gene: AARS2 TMEM151B POLR1C

Linked Data

• MyVariant Identifiers: chr6:g.44271052G>C (hg19) ; chr6:g.44303315G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44303315G>C , CM000668.2:g.44303315G>C	GRCh38
NC_000006.11:g.44271052G>C , CM000668.1:g.44271052G>C	GRCh37
NC_000006.10:g.44379030G>C	NCBI36
NG_031952.1:g.15012C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244571.5:c.2116C>G (AARS2) MANE Select	ENSP00000244571.4:p.Gln706Glu
ENST00000244571.4:c.2116C>G (AARS2)	ENSP00000244571.4:p.Gln706Glu
ENST00000438774.2:c.577-3628G>C (TMEM151B)	ENSP00000409337.2:n.577-3628G>C
ENST00000505802.1:c.314-3628G>C
NM_020745.3:c.2116C>G (AARS2)	NP_065796.1:p.Gln706Glu
XM_005249245.2:c.1825C>G (AARS2)	XP_005249302.1:p.Gln609Glu
XM_011514764.1:c.2116C>G (AARS2)	XP_011513066.1:p.Gln706Glu
XR_241907.2:n.2151C>G (AARS2)
XM_005249245.3:c.1825C>G (AARS2)	XP_005249302.1:p.Gln609Glu
XM_011514764.2:c.2116C>G (AARS2)	XP_011513066.1:p.Gln706Glu
XM_017011112.1:c.826C>G (AARS2)	XP_016866601.1:p.Gln276Glu
NM_020745.4:c.2116C>G (AARS2) MANE Select	NP_065796.2:p.Gln706Glu
NM_001318876.2:c.946-138575G>C (POLR1C)	NP_001305805.1:n.946-138575G>C