Canonical Allele Identifier: CA831789159

Gene: FOXP2

Linked Data

• dbSNP Id: rs1283087180
• gnomAD v3: 7-114101089-T-C
• gnomAD v4: 7-114101089-T-C
• MyVariant Identifiers: chr7:g.113741144T>C (hg19) ; chr7:g.114101089T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114101089T>C , CM000669.2:g.114101089T>C	GRCh38
NC_000007.13:g.113741144T>C , CM000669.1:g.113741144T>C	GRCh37
NC_000007.12:g.113528380T>C	NCBI36
NG_007491.2:g.19780T>C
NG_007491.3:g.19780T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000703612.1:c.-247+14478T>C	ENSP00000515396.1:n.-247+14478T>C
ENST00000703613.1:c.-365+14478T>C	ENSP00000515397.1:n.-365+14478T>C
ENST00000703614.1:c.-247+14478T>C	ENSP00000515398.1:n.-247+14478T>C
ENST00000703615.1:c.-365+14478T>C	ENSP00000515399.1:n.-365+14478T>C
ENST00000703616.1:c.-247+13251T>C	ENSP00000515400.1:n.-247+13251T>C
ENST00000412402.5:c.-102+14478T>C	ENSP00000405470.1:n.-102+14478T>C
ENST00000440349.5:c.-247+14478T>C	ENSP00000395552.1:n.-247+14478T>C
ENST00000441290.6:c.-435+14478T>C	ENSP00000416825.1:n.-435+14478T>C
ENST00000495516.1:n.105+12819T>C
ENST00000635638.1:c.-247+13251T>C	ENSP00000489073.1:n.-247+13251T>C
NR_033766.1:n.302+14478T>C
XM_011516706.1:c.-360+14478T>C	XP_011515008.1:n.-360+14478T>C
XM_017012801.2:c.-247+12661T>C	XP_016868290.1:n.-247+12661T>C
NR_033766.2:n.285+14478T>C