Canonical Allele Identifier: CA364336794

Gene: AARS2 TMEM151B POLR1C

Linked Data

• ClinVar Variation Id: 1685483
• ClinVar RCV Id: RCV002249210
• dbSNP Id: rs2153353848
• MyVariant Identifiers: chr6:g.44270127C>G (hg19) ; chr6:g.44302390C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44302390C>G , CM000668.2:g.44302390C>G	GRCh38
NC_000006.11:g.44270127C>G , CM000668.1:g.44270127C>G	GRCh37
NC_000006.10:g.44378105C>G	NCBI36
NG_031952.1:g.15937G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244571.5:c.2487+1G>C (AARS2) MANE Select	ENSP00000244571.4:n.2487+1G>C
ENST00000244571.4:c.2487+1G>C (AARS2)	ENSP00000244571.4:n.2487+1G>C
ENST00000438774.2:c.577-4553C>G (TMEM151B)	ENSP00000409337.2:n.577-4553C>G
ENST00000505802.1:c.314-4553C>G
NM_020745.3:c.2487+1G>C (AARS2)	NP_065796.1:n.2487+1G>C
XM_005249245.2:c.2196+1G>C (AARS2)	XP_005249302.1:n.2196+1G>C
XM_011514764.1:c.2487+1G>C (AARS2)	XP_011513066.1:n.2487+1G>C
XR_241907.2:n.2412+1G>C (AARS2)
XM_005249245.3:c.2196+1G>C (AARS2)	XP_005249302.1:n.2196+1G>C
XM_011514764.2:c.2487+1G>C (AARS2)	XP_011513066.1:n.2487+1G>C
XM_017011112.1:c.1197+1G>C (AARS2)	XP_016866601.1:n.1197+1G>C
NM_020745.4:c.2487+1G>C (AARS2) MANE Select	NP_065796.2:n.2487+1G>C
NM_001318876.2:c.946-139500C>G (POLR1C)	NP_001305805.1:n.946-139500C>G