Canonical Allele Identifier: CA450316615

Gene: AARS2 TMEM151B POLR1C

Linked Data

• MyVariant Identifiers: chr6:g.44272816G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44305079G>A , CM000668.2:g.44305079G>A	GRCh38
NC_000006.11:g.44272816G>A , CM000668.1:g.44272816G>A	GRCh37
NC_000006.10:g.44380794G>A	NCBI36
NG_031952.1:g.13248C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244571.5:c.1554C>T (AARS2) MANE Select	ENSP00000244571.4:p.Tyr518=
ENST00000244571.4:c.1554C>T (AARS2)	ENSP00000244571.4:p.Tyr518=
ENST00000438774.2:c.577-1864G>A (TMEM151B)	ENSP00000409337.2:n.577-1864G>A
ENST00000505802.1:c.314-1864G>A
NM_020745.3:c.1554C>T (AARS2)	NP_065796.1:p.Tyr518=
XM_005249245.2:c.1263C>T (AARS2)	XP_005249302.1:p.Tyr421=
XM_011514764.1:c.1554C>T (AARS2)	XP_011513066.1:p.Tyr518=
XR_241907.2:n.1589C>T (AARS2)
XM_005249245.3:c.1263C>T (AARS2)	XP_005249302.1:p.Tyr421=
XM_011514764.2:c.1554C>T (AARS2)	XP_011513066.1:p.Tyr518=
XM_017011112.1:c.264C>T (AARS2)	XP_016866601.1:p.Tyr88=
NM_020745.4:c.1554C>T (AARS2) MANE Select	NP_065796.2:p.Tyr518=
NM_001318876.2:c.946-136811G>A (POLR1C)	NP_001305805.1:n.946-136811G>A