Canonical Allele Identifier: CA364336968

Gene: AARS2 TMEM151B POLR1C

Linked Data

• gnomAD v4: 6-44302474-C-T
• MyVariant Identifiers: chr6:g.44270211C>T (hg19) ; chr6:g.44302474C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44302474C>T , CM000668.2:g.44302474C>T	GRCh38
NC_000006.11:g.44270211C>T , CM000668.1:g.44270211C>T	GRCh37
NC_000006.10:g.44378189C>T	NCBI36
NG_031952.1:g.15853G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244571.5:c.2404G>A (AARS2) MANE Select	ENSP00000244571.4:p.Ala802Thr
ENST00000244571.4:c.2404G>A (AARS2)	ENSP00000244571.4:p.Ala802Thr
ENST00000438774.2:c.577-4469C>T (TMEM151B)	ENSP00000409337.2:n.577-4469C>T
ENST00000505802.1:c.314-4469C>T
NM_020745.3:c.2404G>A (AARS2)	NP_065796.1:p.Ala802Thr
XM_005249245.2:c.2113G>A (AARS2)	XP_005249302.1:p.Ala705Thr
XM_011514764.1:c.2404G>A (AARS2)	XP_011513066.1:p.Ala802Thr
XR_241907.2:n.2329G>A (AARS2)
XM_005249245.3:c.2113G>A (AARS2)	XP_005249302.1:p.Ala705Thr
XM_011514764.2:c.2404G>A (AARS2)	XP_011513066.1:p.Ala802Thr
XM_017011112.1:c.1114G>A (AARS2)	XP_016866601.1:p.Ala372Thr
NM_020745.4:c.2404G>A (AARS2) MANE Select	NP_065796.2:p.Ala802Thr
NM_001318876.2:c.946-139416C>T (POLR1C)	NP_001305805.1:n.946-139416C>T