Canonical Allele Identifier: CA1106299956

Gene: CFTR

Linked Data

• dbSNP Id: rs1797945862
• gnomAD v3: 7-117479311-G-A
• gnomAD v4: 7-117479311-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117479311G>A , CM000669.2:g.117479311G>A	GRCh38
NC_000007.13:g.117119365G>A , CM000669.1:g.117119365G>A	GRCh37
NC_000007.12:g.116906601G>A	NCBI36
NG_016465.4:g.18528G>A , LRG_663:g.18528G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446805.2:c.-458G>A	ENSP00000417012.1:n.-458G>A
ENST00000673785.1:c.-406+13480G>A	ENSP00000501235.1:n.-406+13480G>A
ENST00000446805.1:c.-458G>A	ENSP00000417012.1:n.-458G>A
ENST00000546407.1:n.166+3503G>A
XM_011515751.1:c.109G>A	XP_011514053.1:p.Gly37Ser
XM_011515752.1:c.109G>A	XP_011514054.1:p.Gly37Ser
XM_011515753.1:c.-458G>A	XP_011514055.1:n.-458G>A
XM_011515754.1:c.-786G>A	XP_011514056.1:n.-786G>A