Canonical Allele Identifier: CA138384670

Gene: AARS2 TMEM151B POLR1C

Linked Data

• dbSNP Id: rs750031143
• MyVariant Identifiers: chr6:g.44269526G>C (hg19) ; chr6:g.44301789G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44301789G>C , CM000668.2:g.44301789G>C	GRCh38
NC_000006.11:g.44269526G>C , CM000668.1:g.44269526G>C	GRCh37
NC_000006.10:g.44377504G>C	NCBI36
NG_031952.1:g.16538C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244571.5:c.2598+271C>G (AARS2) MANE Select	ENSP00000244571.4:n.2598+271C>G
ENST00000244571.4:c.2598+271C>G (AARS2)	ENSP00000244571.4:n.2598+271C>G
ENST00000438774.2:c.577-5154G>C (TMEM151B)	ENSP00000409337.2:n.577-5154G>C
ENST00000505802.1:c.314-5154G>C
NM_020745.3:c.2598+271C>G (AARS2)	NP_065796.1:n.2598+271C>G
XM_005249245.2:c.2307+271C>G (AARS2)	XP_005249302.1:n.2307+271C>G
XM_011514764.1:c.2598+271C>G (AARS2)	XP_011513066.1:n.2598+271C>G
XR_241907.2:n.2523+271C>G (AARS2)
XM_005249245.3:c.2307+271C>G (AARS2)	XP_005249302.1:n.2307+271C>G
XM_011514764.2:c.2598+271C>G (AARS2)	XP_011513066.1:n.2598+271C>G
XM_017011112.1:c.1308+271C>G (AARS2)	XP_016866601.1:n.1308+271C>G
NM_020745.4:c.2598+271C>G (AARS2) MANE Select	NP_065796.2:n.2598+271C>G
NM_001318876.2:c.946-140101G>C (POLR1C)	NP_001305805.1:n.946-140101G>C