Canonical Allele Identifier: CA1941453790
Community Standard Title: NM_001099667.3(ARMS2):c.112C= (p.Arg38=)
Gene: ARMS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122454839C= , CM000672.2:g.122454839C= GRCh38
NC_000010.10:g.124214355C= , CM000672.1:g.124214355C= GRCh37
NC_000010.9:g.124204345C= NCBI36
NG_011725.1:g.5177C=

Transcript Alleles

HGVS Amino-acid Change
NM_001099667.3:c.112C= MANE Select NP_001093137.1:p.Arg38=
ENST00000528446.1:c.112C= MANE Select ENSP00000436682.1:p.Arg38=
NM_001099667.1:c.112C= NP_001093137.1:p.Arg38=
NM_001099667.2:c.112C= NP_001093137.1:p.Arg38=
XR_946382.1:n.1827+3656G=
XR_946382.2:n.1855+3656G=
XR_946383.1:n.1827+3656G=
XR_946383.2:n.1855+3656G=
XR_946384.1:n.1576+3656G=
XR_946384.2:n.1580+3656G=