Canonical Allele Identifier: CA831842224

Gene: FOXP2

Linked Data

• dbSNP Id: rs1401877311
• gnomAD v3: 7-114337998-C-T
• gnomAD v4: 7-114337998-C-T
• MyVariant Identifiers: chr7:g.113978053C>T (hg19) ; chr7:g.114337998C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114337998C>T , CM000669.2:g.114337998C>T	GRCh38
NC_000007.13:g.113978053C>T , CM000669.1:g.113978053C>T	GRCh37
NC_000007.12:g.113765289C>T	NCBI36
NG_007491.2:g.256689C>T
NG_007491.3:g.256689C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000703612.1:c.-11+49889C>T	ENSP00000515396.1:n.-11+49889C>T
ENST00000703613.1:c.-11+49889C>T	ENSP00000515397.1:n.-11+49889C>T
ENST00000703614.1:c.-11+49889C>T	ENSP00000515398.1:n.-11+49889C>T
ENST00000703615.1:c.-11+49889C>T	ENSP00000515399.1:n.-11+49889C>T
ENST00000703616.1:c.-11+49889C>T	ENSP00000515400.1:n.-11+49889C>T
ENST00000412402.5:c.-11+49889C>T	ENSP00000405470.1:n.-11+49889C>T
ENST00000440349.5:c.-11+49889C>T	ENSP00000395552.1:n.-11+49889C>T
ENST00000441290.6:c.-146-28507C>T	ENSP00000416825.1:n.-146-28507C>T
ENST00000495516.1:n.341+49889C>T
ENST00000634411.1:c.-11+49889C>T	ENSP00000489135.1:n.-11+49889C>T
ENST00000634623.1:c.-11+49889C>T	ENSP00000488944.1:n.-11+49889C>T
ENST00000635109.1:c.-11+49889C>T	ENSP00000489457.1:n.-11+49889C>T
ENST00000635638.1:c.-11+49889C>T	ENSP00000489073.1:n.-11+49889C>T
NR_033766.1:n.393+49889C>T
XM_011516706.1:c.-11+17928C>T	XP_011515008.1:n.-11+17928C>T
XM_017012801.2:c.-11+49889C>T	XP_016868290.1:n.-11+49889C>T
NR_033766.2:n.376+49889C>T