Canonical Allele Identifier: CA164948474

Gene: CFTR

Linked Data

• dbSNP Id: rs992706998
• gnomAD v2: 7-117119646-G-T
• gnomAD v3: 7-117479592-G-T
• gnomAD v4: 7-117479592-G-T
• MyVariant Identifiers: chr7:g.117119646G>T (hg19) ; chr7:g.117479592G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117479592G>T , CM000669.2:g.117479592G>T	GRCh38
NC_000007.13:g.117119646G>T , CM000669.1:g.117119646G>T	GRCh37
NC_000007.12:g.116906882G>T	NCBI36
NG_016465.4:g.18809G>T , LRG_663:g.18809G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446805.2:c.-293G>T	ENSP00000417012.1:n.-293G>T
ENST00000673785.1:c.-406+13761G>T	ENSP00000501235.1:n.-406+13761G>T
ENST00000446805.1:c.-293G>T	ENSP00000417012.1:n.-293G>T
ENST00000546407.1:n.166+3784G>T
XM_011515751.1:c.143+247G>T	XP_011514053.1:n.143+247G>T
XM_011515752.1:c.143+247G>T	XP_011514054.1:n.143+247G>T
XM_011515753.1:c.-293G>T	XP_011514055.1:n.-293G>T
XM_011515754.1:c.-621G>T	XP_011514056.1:n.-621G>T