Canonical Allele Identifier: CA364341903

Gene: AARS2 POLR1C

Linked Data

• gnomAD v4: 6-44313087-C-T
• MyVariant Identifiers: chr6:g.44280824C>T (hg19) ; chr6:g.44313087C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44313087C>T , CM000668.2:g.44313087C>T	GRCh38
NC_000006.11:g.44280824C>T , CM000668.1:g.44280824C>T	GRCh37
NC_000006.10:g.44388802C>T	NCBI36
NG_031952.1:g.5240G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000244571.5:c.237G>A (AARS2) MANE Select	ENSP00000244571.4:p.Met79Ile
ENST00000244571.4:c.237G>A (AARS2)	ENSP00000244571.4:p.Met79Ile
ENST00000505802.1:c.855+5445C>T
NM_020745.3:c.237G>A (AARS2)	NP_065796.1:p.Met79Ile
XM_005249245.2:c.237G>A (AARS2)	XP_005249302.1:p.Met79Ile
XM_011514764.1:c.237G>A (AARS2)	XP_011513066.1:p.Met79Ile
XR_241907.2:n.272G>A (AARS2)
XM_005249245.3:c.237G>A (AARS2)	XP_005249302.1:p.Met79Ile
XM_011514764.2:c.237G>A (AARS2)	XP_011513066.1:p.Met79Ile
XM_017011112.1:c.-782G>A (AARS2)	XP_016866601.1:n.-782G>A
NM_020745.4:c.237G>A (AARS2) MANE Select	NP_065796.2:p.Met79Ile
NM_001318876.2:c.946-128803C>T (POLR1C)	NP_001305805.1:n.946-128803C>T