Canonical Allele Identifier: CA450316004

Gene: AARS2 TMEM151B POLR1C

Linked Data

• gnomAD v4: 6-44302147-G-C
• MyVariant Identifiers: chr6:g.44269884G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44302147G>C , CM000668.2:g.44302147G>C	GRCh38
NC_000006.11:g.44269884G>C , CM000668.1:g.44269884G>C	GRCh37
NC_000006.10:g.44377862G>C	NCBI36
NG_031952.1:g.16180C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244571.5:c.2511C>G (AARS2) MANE Select	ENSP00000244571.4:p.Pro837=
ENST00000244571.4:c.2511C>G (AARS2)	ENSP00000244571.4:p.Pro837=
ENST00000438774.2:c.577-4796G>C (TMEM151B)	ENSP00000409337.2:n.577-4796G>C
ENST00000505802.1:c.314-4796G>C
NM_020745.3:c.2511C>G (AARS2)	NP_065796.1:p.Pro837=
XM_005249245.2:c.2220C>G (AARS2)	XP_005249302.1:p.Pro740=
XM_011514764.1:c.2511C>G (AARS2)	XP_011513066.1:p.Pro837=
XR_241907.2:n.2436C>G (AARS2)
XM_005249245.3:c.2220C>G (AARS2)	XP_005249302.1:p.Pro740=
XM_011514764.2:c.2511C>G (AARS2)	XP_011513066.1:p.Pro837=
XM_017011112.1:c.1221C>G (AARS2)	XP_016866601.1:p.Pro407=
NM_020745.4:c.2511C>G (AARS2) MANE Select	NP_065796.2:p.Pro837=
NM_001318876.2:c.946-139743G>C (POLR1C)	NP_001305805.1:n.946-139743G>C