Canonical Allele Identifier: CA2026286726
Gene: YARS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32755719G= , CM000674.2:g.32755719G= GRCh38
NC_000012.11:g.32908653G= , CM000674.1:g.32908653G= GRCh37
NC_000012.10:g.32799920G= NCBI36
NG_028122.1:g.5235C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000324868.13:c.156C= MANE Select ENSP00000320658.8:p.Phe52=
ENST00000324868.12:c.156C= ENSP00000320658.8:p.Phe52=
ENST00000548490.1:c.78C= ENSP00000447710.1:p.Phe26=
NM_001040436.2:c.156C= NP_001035526.1:p.Phe52=
XR_242891.3:n.243C=
XR_242892.3:n.243C=
XR_429036.1:n.243C=
XR_931296.1:n.243C=
XR_931297.1:n.243C=
XR_931298.1:n.243C=
XR_931299.1:n.243C=
XR_001748730.2:n.740C=
XR_002957331.1:n.740C=
XR_242892.5:n.740C=
XR_931296.3:n.740C=
NM_001040436.3:c.156C= MANE Select NP_001035526.1:p.Phe52=