Canonical Allele Identifier: CA2678954372

Linked Data

gnomAD v4: 6-44305010-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44305010G>A , CM000668.2:g.44305010G>A GRCh38
NC_000006.11:g.44272747G>A , CM000668.1:g.44272747G>A GRCh37
NC_000006.10:g.44380725G>A NCBI36
NG_031952.1:g.13317C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000244571.5:c.1579+44C>T (AARS2) MANE Select ENSP00000244571.4:n.1579+44C>T
ENST00000244571.4:c.1579+44C>T (AARS2) ENSP00000244571.4:n.1579+44C>T
ENST00000438774.2:c.577-1933G>A (TMEM151B) ENSP00000409337.2:n.577-1933G>A
ENST00000505802.1:c.314-1933G>A
NM_020745.3:c.1579+44C>T (AARS2) NP_065796.1:n.1579+44C>T
XM_005249245.2:c.1288+44C>T (AARS2) XP_005249302.1:n.1288+44C>T
XM_011514764.1:c.1579+44C>T (AARS2) XP_011513066.1:n.1579+44C>T
XR_241907.2:n.1614+44C>T (AARS2)
XM_005249245.3:c.1288+44C>T (AARS2) XP_005249302.1:n.1288+44C>T
XM_011514764.2:c.1579+44C>T (AARS2) XP_011513066.1:n.1579+44C>T
XM_017011112.1:c.289+44C>T (AARS2) XP_016866601.1:n.289+44C>T
NM_020745.4:c.1579+44C>T (AARS2) MANE Select NP_065796.2:n.1579+44C>T
NM_001318876.2:c.946-136880G>A (POLR1C) NP_001305805.1:n.946-136880G>A