Canonical Allele Identifier: CA1941454129

Gene: ARMS2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122455772C= , CM000672.2:g.122455772C=	GRCh38
NC_000010.10:g.124215288C= , CM000672.1:g.124215288C=	GRCh37
NC_000010.9:g.124205278C=	NCBI36
NG_011725.1:g.6110C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000528446.1:c.297+748C= MANE Select	ENSP00000436682.1:n.297+748C=
NM_001099667.1:c.297+748C=	NP_001093137.1:n.297+748C=
XR_946382.1:n.1827+2723G=
XR_946383.1:n.1827+2723G=
XR_946384.1:n.1576+2723G=
XR_946385.1:n.1828-751G=
NM_001099667.2:c.297+748C=	NP_001093137.1:n.297+748C=
XR_946382.2:n.1855+2723G=
XR_946383.2:n.1855+2723G=
XR_946384.2:n.1580+2723G=
XR_946385.2:n.1856-751G=
NM_001099667.3:c.297+748C= MANE Select	NP_001093137.1:n.297+748C=