Canonical Allele Identifier: CA450391903
Gene: AARS2 HGNC NCBI
POLR1C HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.44280926G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44313189G>T , CM000668.2:g.44313189G>T GRCh38
NC_000006.11:g.44280926G>T , CM000668.1:g.44280926G>T GRCh37
NC_000006.10:g.44388904G>T NCBI36
NG_031952.1:g.5138C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000244571.5:c.135C>A (AARS2) MANE Select ENSP00000244571.4:p.Ala45=
ENST00000244571.4:c.135C>A (AARS2) ENSP00000244571.4:p.Ala45=
ENST00000505802.1:c.855+5547G>T
NM_020745.3:c.135C>A (AARS2) NP_065796.1:p.Ala45=
XM_005249245.2:c.135C>A (AARS2) XP_005249302.1:p.Ala45=
XM_011514764.1:c.135C>A (AARS2) XP_011513066.1:p.Ala45=
XR_241907.2:n.170C>A (AARS2)
XM_005249245.3:c.135C>A (AARS2) XP_005249302.1:p.Ala45=
XM_011514764.2:c.135C>A (AARS2) XP_011513066.1:p.Ala45=
NM_020745.4:c.135C>A (AARS2) MANE Select NP_065796.2:p.Ala45=
NM_001318876.2:c.946-128701G>T (POLR1C) NP_001305805.1:n.946-128701G>T