Canonical Allele Identifier: CA1941453826
Gene: ARMS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122454937A= , CM000672.2:g.122454937A= GRCh38
NC_000010.10:g.124214453A= , CM000672.1:g.124214453A= GRCh37
NC_000010.9:g.124204443A= NCBI36
NG_011725.1:g.5275A=

Transcript Alleles

HGVS Amino-acid change
ENST00000528446.1:c.210A= MANE Select ENSP00000436682.1:p.Lys70=
NM_001099667.1:c.210A= NP_001093137.1:p.Lys70=
XR_946382.1:n.1827+3558T=
XR_946383.1:n.1827+3558T=
XR_946384.1:n.1576+3558T=
XR_946385.1:n.1912T=
NM_001099667.2:c.210A= NP_001093137.1:p.Lys70=
XR_946382.2:n.1855+3558T=
XR_946383.2:n.1855+3558T=
XR_946384.2:n.1580+3558T=
XR_946385.2:n.1940T=
NM_001099667.3:c.210A= MANE Select NP_001093137.1:p.Lys70=