Canonical Allele Identifier: CA824984859

Gene: AARS2 TMEM151B POLR1C

Linked Data

• dbSNP Id: rs1416920473
• gnomAD v3: 6-44302622-A-G
• gnomAD v4: 6-44302622-A-G
• MyVariant Identifiers: chr6:g.44270359A>G (hg19) ; chr6:g.44302622A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44302622A>G , CM000668.2:g.44302622A>G	GRCh38
NC_000006.11:g.44270359A>G , CM000668.1:g.44270359A>G	GRCh37
NC_000006.10:g.44378337A>G	NCBI36
NG_031952.1:g.15705T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244571.5:c.2365-109T>C (AARS2) MANE Select	ENSP00000244571.4:n.2365-109T>C
ENST00000244571.4:c.2365-109T>C (AARS2)	ENSP00000244571.4:n.2365-109T>C
ENST00000438774.2:c.577-4321A>G (TMEM151B)	ENSP00000409337.2:n.577-4321A>G
ENST00000505802.1:c.314-4321A>G
NM_020745.3:c.2365-109T>C (AARS2)	NP_065796.1:n.2365-109T>C
XM_005249245.2:c.2074-109T>C (AARS2)	XP_005249302.1:n.2074-109T>C
XM_011514764.1:c.2365-109T>C (AARS2)	XP_011513066.1:n.2365-109T>C
XR_241907.2:n.2290-109T>C (AARS2)
XM_005249245.3:c.2074-109T>C (AARS2)	XP_005249302.1:n.2074-109T>C
XM_011514764.2:c.2365-109T>C (AARS2)	XP_011513066.1:n.2365-109T>C
XM_017011112.1:c.1075-109T>C (AARS2)	XP_016866601.1:n.1075-109T>C
NM_020745.4:c.2365-109T>C (AARS2) MANE Select	NP_065796.2:n.2365-109T>C
NM_001318876.2:c.946-139268A>G (POLR1C)	NP_001305805.1:n.946-139268A>G