Canonical Allele Identifier: CA364335428

Gene: AARS2 TMEM151B POLR1C

Linked Data

• gnomAD v4: 6-44300571-T-G
• MyVariant Identifiers: chr6:g.44268308T>G (hg19) ; chr6:g.44300571T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44300571T>G , CM000668.2:g.44300571T>G	GRCh38
NC_000006.11:g.44268308T>G , CM000668.1:g.44268308T>G	GRCh37
NC_000006.10:g.44376286T>G	NCBI36
NG_031952.1:g.17756A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244571.5:c.2934A>C (AARS2) MANE Select	ENSP00000244571.4:p.Gln978His
ENST00000244571.4:c.2934A>C (AARS2)	ENSP00000244571.4:p.Gln978His
ENST00000438774.2:c.577-6372T>G (TMEM151B)	ENSP00000409337.2:n.577-6372T>G
ENST00000505802.1:c.314-6372T>G
NM_020745.3:c.2934A>C (AARS2)	NP_065796.1:p.Gln978His
XM_005249245.2:c.2643A>C (AARS2)	XP_005249302.1:p.Gln881His
XM_011514764.1:c.2793+585A>C (AARS2)	XP_011513066.1:n.2793+585A>C
XR_241907.2:n.2859A>C (AARS2)
XM_005249245.3:c.2643A>C (AARS2)	XP_005249302.1:p.Gln881His
XM_011514764.2:c.2793+585A>C (AARS2)	XP_011513066.1:n.2793+585A>C
XM_017011112.1:c.1644A>C (AARS2)	XP_016866601.1:p.Gln548His
NM_020745.4:c.2934A>C (AARS2) MANE Select	NP_065796.2:p.Gln978His
NM_001318876.2:c.946-141319T>G (POLR1C)	NP_001305805.1:n.946-141319T>G