Canonical Allele Identifier: CA6955916

Gene: FREM2

Linked Data

• ClinVar Variation Id: 312018
• ClinVar RCV Id: RCV000323344 ; RCV001701949 ; RCV002056384
• dbSNP Id: rs200338297
• ExAC: 13:39435638 C / T
• gnomAD v2: 13-39435638-C-T
• gnomAD v3: 13-38861501-C-T
• gnomAD v4: 13-38861501-C-T
• MyVariant Identifiers: chr13:g.39435638C>T (hg19) ; chr13:g.38861501C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.38861501C>T , CM000675.2:g.38861501C>T	GRCh38
NC_000013.10:g.39435638C>T , CM000675.1:g.39435638C>T	GRCh37
NC_000013.9:g.38333638C>T	NCBI36
NG_008125.2:g.179466C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280481.9:c.7590C>T MANE Select	ENSP00000280481.7:p.Gly2530=
ENST00000280481.8:c.7590C>T	ENSP00000280481.7:p.Gly2530=
NM_207361.5:c.7590C>T	NP_997244.4:p.Gly2530=
NM_207361.6:c.7590C>T MANE Select	NP_997244.4:p.Gly2530=