Canonical Allele Identifier: CA1737343590

Gene: CFTR

Linked Data

• dbSNP Id: rs1797935393

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117478978A>G , CM000669.2:g.117478978A>G	GRCh38
NC_000007.13:g.117119032A>G , CM000669.1:g.117119032A>G	GRCh37
NC_000007.12:g.116906268A>G	NCBI36
NG_016465.4:g.18195A>G , LRG_663:g.18195A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446805.2:c.-525-266A>G	ENSP00000417012.1:n.-525-266A>G
ENST00000673785.1:c.-406+13147A>G	ENSP00000501235.1:n.-406+13147A>G
ENST00000546407.1:n.166+3170A>G
XM_011515751.1:c.42-266A>G	XP_011514053.1:n.42-266A>G
XM_011515752.1:c.42-266A>G	XP_011514054.1:n.42-266A>G
XM_011515754.1:c.-1119A>G	XP_011514056.1:n.-1119A>G