Canonical Allele Identifier: CA364338775

Gene: AARS2 TMEM151B POLR1C

Linked Data

• MyVariant Identifiers: chr6:g.44272818A>C (hg19) ; chr6:g.44305081A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44305081A>C , CM000668.2:g.44305081A>C	GRCh38
NC_000006.11:g.44272818A>C , CM000668.1:g.44272818A>C	GRCh37
NC_000006.10:g.44380796A>C	NCBI36
NG_031952.1:g.13246T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244571.5:c.1552T>G (AARS2) MANE Select	ENSP00000244571.4:p.Tyr518Asp
ENST00000244571.4:c.1552T>G (AARS2)	ENSP00000244571.4:p.Tyr518Asp
ENST00000438774.2:c.577-1862A>C (TMEM151B)	ENSP00000409337.2:n.577-1862A>C
ENST00000505802.1:c.314-1862A>C
NM_020745.3:c.1552T>G (AARS2)	NP_065796.1:p.Tyr518Asp
XM_005249245.2:c.1261T>G (AARS2)	XP_005249302.1:p.Tyr421Asp
XM_011514764.1:c.1552T>G (AARS2)	XP_011513066.1:p.Tyr518Asp
XR_241907.2:n.1587T>G (AARS2)
XM_005249245.3:c.1261T>G (AARS2)	XP_005249302.1:p.Tyr421Asp
XM_011514764.2:c.1552T>G (AARS2)	XP_011513066.1:p.Tyr518Asp
XM_017011112.1:c.262T>G (AARS2)	XP_016866601.1:p.Tyr88Asp
NM_020745.4:c.1552T>G (AARS2) MANE Select	NP_065796.2:p.Tyr518Asp
NM_001318876.2:c.946-136809A>C (POLR1C)	NP_001305805.1:n.946-136809A>C