Canonical Allele Identifier: CA378601632
Gene: ARMS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122454944A>T , CM000672.2:g.122454944A>T GRCh38
NC_000010.10:g.124214460A>T , CM000672.1:g.124214460A>T GRCh37
NC_000010.9:g.124204450A>T NCBI36
NG_011725.1:g.5282A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000528446.1:c.217A>T MANE Select ENSP00000436682.1:p.Thr73Ser
NM_001099667.1:c.217A>T NP_001093137.1:p.Thr73Ser
XR_946382.1:n.1827+3551T>A
XR_946383.1:n.1827+3551T>A
XR_946384.1:n.1576+3551T>A
XR_946385.1:n.1905T>A
NM_001099667.2:c.217A>T NP_001093137.1:p.Thr73Ser
XR_946382.2:n.1855+3551T>A
XR_946383.2:n.1855+3551T>A
XR_946384.2:n.1580+3551T>A
XR_946385.2:n.1933T>A
NM_001099667.3:c.217A>T MANE Select NP_001093137.1:p.Thr73Ser