Canonical Allele Identifier: CA1941453829
Gene: ARMS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122454943C= , CM000672.2:g.122454943C= GRCh38
NC_000010.10:g.124214459C= , CM000672.1:g.124214459C= GRCh37
NC_000010.9:g.124204449C= NCBI36
NG_011725.1:g.5281C=

Transcript Alleles

HGVS Amino-acid change
ENST00000528446.1:c.216C= MANE Select ENSP00000436682.1:p.His72=
NM_001099667.1:c.216C= NP_001093137.1:p.His72=
XR_946382.1:n.1827+3552G=
XR_946383.1:n.1827+3552G=
XR_946384.1:n.1576+3552G=
XR_946385.1:n.1906G=
NM_001099667.2:c.216C= NP_001093137.1:p.His72=
XR_946382.2:n.1855+3552G=
XR_946383.2:n.1855+3552G=
XR_946384.2:n.1580+3552G=
XR_946385.2:n.1934G=
NM_001099667.3:c.216C= MANE Select NP_001093137.1:p.His72=