Canonical Allele Identifier: CA1106299942

Gene: CFTR

Linked Data

• dbSNP Id: rs1797944853
• gnomAD v3: 7-117479288-T-G
• gnomAD v4: 7-117479288-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117479288T>G , CM000669.2:g.117479288T>G	GRCh38
NC_000007.13:g.117119342T>G , CM000669.1:g.117119342T>G	GRCh37
NC_000007.12:g.116906578T>G	NCBI36
NG_016465.4:g.18505T>G , LRG_663:g.18505T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446805.2:c.-481T>G	ENSP00000417012.1:n.-481T>G
ENST00000673785.1:c.-406+13457T>G	ENSP00000501235.1:n.-406+13457T>G
ENST00000546407.1:n.166+3480T>G
XM_011515751.1:c.86T>G	XP_011514053.1:p.Leu29Arg
XM_011515752.1:c.86T>G	XP_011514054.1:p.Leu29Arg
XM_011515754.1:c.-809T>G	XP_011514056.1:n.-809T>G