Canonical Allele Identifier: CA164948496

Gene: CFTR

Linked Data

• dbSNP Id: rs952892489
• gnomAD v3: 7-117479611-T-G
• gnomAD v4: 7-117479611-T-G
• MyVariant Identifiers: chr7:g.117119665T>G (hg19) ; chr7:g.117479611T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117479611T>G , CM000669.2:g.117479611T>G	GRCh38
NC_000007.13:g.117119665T>G , CM000669.1:g.117119665T>G	GRCh37
NC_000007.12:g.116906901T>G	NCBI36
NG_016465.4:g.18828T>G , LRG_663:g.18828T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446805.2:c.-274T>G	ENSP00000417012.1:n.-274T>G
ENST00000673785.1:c.-406+13780T>G	ENSP00000501235.1:n.-406+13780T>G
ENST00000446805.1:c.-274T>G	ENSP00000417012.1:n.-274T>G
ENST00000546407.1:n.166+3803T>G
XM_011515751.1:c.143+266T>G	XP_011514053.1:n.143+266T>G
XM_011515752.1:c.143+266T>G	XP_011514054.1:n.143+266T>G
XM_011515753.1:c.-274T>G	XP_011514055.1:n.-274T>G
XM_011515754.1:c.-602T>G	XP_011514056.1:n.-602T>G