Canonical Allele Identifier: CA214411524

Gene: ARMS2

Linked Data

• dbSNP Id: rs898790897
• gnomAD v3: 10-122455719-G-T
• gnomAD v4: 10-122455719-G-T
• MyVariant Identifiers: chr10:g.124215235G>T (hg19) ; chr10:g.122455719G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122455719G>T , CM000672.2:g.122455719G>T	GRCh38
NC_000010.10:g.124215235G>T , CM000672.1:g.124215235G>T	GRCh37
NC_000010.9:g.124205225G>T	NCBI36
NG_011725.1:g.6057G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000528446.1:c.297+695G>T MANE Select	ENSP00000436682.1:n.297+695G>T
NM_001099667.1:c.297+695G>T	NP_001093137.1:n.297+695G>T
XR_946382.1:n.1827+2776C>A
XR_946383.1:n.1827+2776C>A
XR_946384.1:n.1576+2776C>A
XR_946385.1:n.1828-698C>A
NM_001099667.2:c.297+695G>T	NP_001093137.1:n.297+695G>T
XR_946382.2:n.1855+2776C>A
XR_946383.2:n.1855+2776C>A
XR_946384.2:n.1580+2776C>A
XR_946385.2:n.1856-698C>A
NM_001099667.3:c.297+695G>T MANE Select	NP_001093137.1:n.297+695G>T