Canonical Allele Identifier: CA2722806097

Gene: ARMS2

Linked Data

• dbSNP Id: rs2097476605

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122455713A>T , CM000672.2:g.122455713A>T	GRCh38
NC_000010.10:g.124215229A>T , CM000672.1:g.124215229A>T	GRCh37
NC_000010.9:g.124205219A>T	NCBI36
NG_011725.1:g.6051A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000528446.1:c.297+689A>T MANE Select	ENSP00000436682.1:n.297+689A>T
NM_001099667.1:c.297+689A>T	NP_001093137.1:n.297+689A>T
XR_946382.1:n.1827+2782T>A
XR_946383.1:n.1827+2782T>A
XR_946384.1:n.1576+2782T>A
XR_946385.1:n.1828-692T>A
NM_001099667.2:c.297+689A>T	NP_001093137.1:n.297+689A>T
XR_946382.2:n.1855+2782T>A
XR_946383.2:n.1855+2782T>A
XR_946384.2:n.1580+2782T>A
XR_946385.2:n.1856-692T>A
NM_001099667.3:c.297+689A>T MANE Select	NP_001093137.1:n.297+689A>T