Canonical Allele Identifier: CA378601643
Gene: ARMS2 HGNC NCBI

Linked Data

dbSNP Id: rs1479532926

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122454945C>A , CM000672.2:g.122454945C>A GRCh38
NC_000010.10:g.124214461C>A , CM000672.1:g.124214461C>A GRCh37
NC_000010.9:g.124204451C>A NCBI36
NG_011725.1:g.5283C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000528446.1:c.218C>A MANE Select ENSP00000436682.1:p.Thr73Asn
NM_001099667.1:c.218C>A NP_001093137.1:p.Thr73Asn
XR_946382.1:n.1827+3550G>T
XR_946383.1:n.1827+3550G>T
XR_946384.1:n.1576+3550G>T
XR_946385.1:n.1904G>T
NM_001099667.2:c.218C>A NP_001093137.1:p.Thr73Asn
XR_946382.2:n.1855+3550G>T
XR_946383.2:n.1855+3550G>T
XR_946384.2:n.1580+3550G>T
XR_946385.2:n.1932G>T
NM_001099667.3:c.218C>A MANE Select NP_001093137.1:p.Thr73Asn