Canonical Allele Identifier: CA831842221

Gene: FOXP2

Linked Data

• dbSNP Id: rs1309660369
• gnomAD v3: 7-114337990-T-C
• gnomAD v4: 7-114337990-T-C
• MyVariant Identifiers: chr7:g.113978045T>C (hg19) ; chr7:g.114337990T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114337990T>C , CM000669.2:g.114337990T>C	GRCh38
NC_000007.13:g.113978045T>C , CM000669.1:g.113978045T>C	GRCh37
NC_000007.12:g.113765281T>C	NCBI36
NG_007491.2:g.256681T>C
NG_007491.3:g.256681T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000703612.1:c.-11+49881T>C	ENSP00000515396.1:n.-11+49881T>C
ENST00000703613.1:c.-11+49881T>C	ENSP00000515397.1:n.-11+49881T>C
ENST00000703614.1:c.-11+49881T>C	ENSP00000515398.1:n.-11+49881T>C
ENST00000703615.1:c.-11+49881T>C	ENSP00000515399.1:n.-11+49881T>C
ENST00000703616.1:c.-11+49881T>C	ENSP00000515400.1:n.-11+49881T>C
ENST00000412402.5:c.-11+49881T>C	ENSP00000405470.1:n.-11+49881T>C
ENST00000440349.5:c.-11+49881T>C	ENSP00000395552.1:n.-11+49881T>C
ENST00000441290.6:c.-146-28515T>C	ENSP00000416825.1:n.-146-28515T>C
ENST00000495516.1:n.341+49881T>C
ENST00000634411.1:c.-11+49881T>C	ENSP00000489135.1:n.-11+49881T>C
ENST00000634623.1:c.-11+49881T>C	ENSP00000488944.1:n.-11+49881T>C
ENST00000635109.1:c.-11+49881T>C	ENSP00000489457.1:n.-11+49881T>C
ENST00000635638.1:c.-11+49881T>C	ENSP00000489073.1:n.-11+49881T>C
NR_033766.1:n.393+49881T>C
XM_011516706.1:c.-11+17920T>C	XP_011515008.1:n.-11+17920T>C
XM_017012801.2:c.-11+49881T>C	XP_016868290.1:n.-11+49881T>C
NR_033766.2:n.376+49881T>C