Canonical Allele Identifier: CA15785854

Gene: FREM2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.38796458G>A , CM000675.2:g.38796458G>A	GRCh38
NC_000013.10:g.39370595G>A , CM000675.1:g.39370595G>A	GRCh37
NC_000013.9:g.38268595G>A	NCBI36
NG_008125.2:g.114423G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280481.9:c.6019+11650G>A MANE Select	ENSP00000280481.7:n.6019+11650G>A
ENST00000280481.8:c.6019+11650G>A	ENSP00000280481.7:n.6019+11650G>A
NM_207361.5:c.6019+11650G>A	NP_997244.4:n.6019+11650G>A
XM_011535057.1:c.6019+11650G>A	XP_011533359.1:n.6019+11650G>A
XR_941571.1:n.6327+11650G>A
XR_941571.2:n.6323+11650G>A
NM_207361.6:c.6019+11650G>A MANE Select	NP_997244.4:n.6019+11650G>A