Canonical Allele Identifier: CA1941454112
Gene: ARMS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122455719G= , CM000672.2:g.122455719G= GRCh38
NC_000010.10:g.124215235G= , CM000672.1:g.124215235G= GRCh37
NC_000010.9:g.124205225G= NCBI36
NG_011725.1:g.6057G=

Transcript Alleles

HGVS Amino-acid change
ENST00000528446.1:c.297+695G= MANE Select ENSP00000436682.1:n.297+695G=
NM_001099667.1:c.297+695G= NP_001093137.1:n.297+695G=
XR_946382.1:n.1827+2776C=
XR_946383.1:n.1827+2776C=
XR_946384.1:n.1576+2776C=
XR_946385.1:n.1828-698C=
NM_001099667.2:c.297+695G= NP_001093137.1:n.297+695G=
XR_946382.2:n.1855+2776C=
XR_946383.2:n.1855+2776C=
XR_946384.2:n.1580+2776C=
XR_946385.2:n.1856-698C=
NM_001099667.3:c.297+695G= MANE Select NP_001093137.1:n.297+695G=
Search 100 bp 5'
Search 100 bp 3'