Canonical Allele Identifier: CA1106076566

Gene: FOXP2

Linked Data

• dbSNP Id: rs1790933265
• gnomAD v3: 7-114100970-C-T
• gnomAD v4: 7-114100970-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114100970C>T , CM000669.2:g.114100970C>T	GRCh38
NC_000007.13:g.113741025C>T , CM000669.1:g.113741025C>T	GRCh37
NC_000007.12:g.113528261C>T	NCBI36
NG_007491.2:g.19661C>T
NG_007491.3:g.19661C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703612.1:c.-247+14359C>T	ENSP00000515396.1:n.-247+14359C>T
ENST00000703613.1:c.-365+14359C>T	ENSP00000515397.1:n.-365+14359C>T
ENST00000703614.1:c.-247+14359C>T	ENSP00000515398.1:n.-247+14359C>T
ENST00000703615.1:c.-365+14359C>T	ENSP00000515399.1:n.-365+14359C>T
ENST00000703616.1:c.-247+13132C>T	ENSP00000515400.1:n.-247+13132C>T
ENST00000412402.5:c.-102+14359C>T	ENSP00000405470.1:n.-102+14359C>T
ENST00000440349.5:c.-247+14359C>T	ENSP00000395552.1:n.-247+14359C>T
ENST00000441290.6:c.-435+14359C>T	ENSP00000416825.1:n.-435+14359C>T
ENST00000495516.1:n.105+12700C>T
ENST00000635638.1:c.-247+13132C>T	ENSP00000489073.1:n.-247+13132C>T
NR_033766.1:n.302+14359C>T
XM_011516706.1:c.-360+14359C>T	XP_011515008.1:n.-360+14359C>T
XM_017012801.2:c.-247+12542C>T	XP_016868290.1:n.-247+12542C>T
NR_033766.2:n.285+14359C>T