Canonical Allele Identifier: CA2684616386
Gene: CFTR HGNC NCBI

Linked Data

gnomAD v4: 7-117479459-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117479459C>A , CM000669.2:g.117479459C>A GRCh38
NC_000007.13:g.117119513C>A , CM000669.1:g.117119513C>A GRCh37
NC_000007.12:g.116906749C>A NCBI36
NG_016465.4:g.18676C>A , LRG_663:g.18676C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-423-3C>A ENSP00000417012.1:n.-423-3C>A
ENST00000673785.1:c.-406+13628C>A ENSP00000501235.1:n.-406+13628C>A
ENST00000446805.1:c.-423-3C>A ENSP00000417012.1:n.-423-3C>A
ENST00000546407.1:n.166+3651C>A
XM_011515751.1:c.143+114C>A XP_011514053.1:n.143+114C>A
XM_011515752.1:c.143+114C>A XP_011514054.1:n.143+114C>A
XM_011515753.1:c.-423-3C>A XP_011514055.1:n.-423-3C>A
XM_011515754.1:c.-751-3C>A XP_011514056.1:n.-751-3C>A
Search 100 bp 5'
Search 100 bp 3'