Canonical Allele Identifier: CA378601555
Gene: ARMS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122454935A>C , CM000672.2:g.122454935A>C GRCh38
NC_000010.10:g.124214451A>C , CM000672.1:g.124214451A>C GRCh37
NC_000010.9:g.124204441A>C NCBI36
NG_011725.1:g.5273A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000528446.1:c.208A>C MANE Select ENSP00000436682.1:p.Lys70Gln
NM_001099667.1:c.208A>C NP_001093137.1:p.Lys70Gln
XR_946382.1:n.1827+3560T>G
XR_946383.1:n.1827+3560T>G
XR_946384.1:n.1576+3560T>G
XR_946385.1:n.1914T>G
NM_001099667.2:c.208A>C NP_001093137.1:p.Lys70Gln
XR_946382.2:n.1855+3560T>G
XR_946383.2:n.1855+3560T>G
XR_946384.2:n.1580+3560T>G
XR_946385.2:n.1942T>G
NM_001099667.3:c.208A>C MANE Select NP_001093137.1:p.Lys70Gln