Canonical Allele Identifier: CA824984121

Gene: AARS2 TMEM151B POLR1C

Linked Data

• dbSNP Id: rs191792373
• gnomAD v3: 6-44302012-C-T
• gnomAD v4: 6-44302012-C-T
• MyVariant Identifiers: chr6:g.44269749C>T (hg19) ; chr6:g.44302012C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44302012C>T , CM000668.2:g.44302012C>T	GRCh38
NC_000006.11:g.44269749C>T , CM000668.1:g.44269749C>T	GRCh37
NC_000006.10:g.44377727C>T	NCBI36
NG_031952.1:g.16315G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000244571.5:c.2598+48G>A (AARS2) MANE Select	ENSP00000244571.4:n.2598+48G>A
ENST00000244571.4:c.2598+48G>A (AARS2)	ENSP00000244571.4:n.2598+48G>A
ENST00000438774.2:c.577-4931C>T (TMEM151B)	ENSP00000409337.2:n.577-4931C>T
ENST00000505802.1:c.314-4931C>T
NM_020745.3:c.2598+48G>A (AARS2)	NP_065796.1:n.2598+48G>A
XM_005249245.2:c.2307+48G>A (AARS2)	XP_005249302.1:n.2307+48G>A
XM_011514764.1:c.2598+48G>A (AARS2)	XP_011513066.1:n.2598+48G>A
XR_241907.2:n.2523+48G>A (AARS2)
XM_005249245.3:c.2307+48G>A (AARS2)	XP_005249302.1:n.2307+48G>A
XM_011514764.2:c.2598+48G>A (AARS2)	XP_011513066.1:n.2598+48G>A
XM_017011112.1:c.1308+48G>A (AARS2)	XP_016866601.1:n.1308+48G>A
NM_020745.4:c.2598+48G>A (AARS2) MANE Select	NP_065796.2:n.2598+48G>A
NM_001318876.2:c.946-139878C>T (POLR1C)	NP_001305805.1:n.946-139878C>T