Canonical Allele Identifier: CA1737343711
Gene: CFTR HGNC NCBI

Linked Data

dbSNP Id: rs1584763877

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117479199C>A , CM000669.2:g.117479199C>A GRCh38
NC_000007.13:g.117119253C>A , CM000669.1:g.117119253C>A GRCh37
NC_000007.12:g.116906489C>A NCBI36
NG_016465.4:g.18416C>A , LRG_663:g.18416C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-525-45C>A ENSP00000417012.1:n.-525-45C>A
ENST00000673785.1:c.-406+13368C>A ENSP00000501235.1:n.-406+13368C>A
ENST00000546407.1:n.166+3391C>A
XM_011515751.1:c.42-45C>A XP_011514053.1:n.42-45C>A
XM_011515752.1:c.42-45C>A XP_011514054.1:n.42-45C>A
XM_011515754.1:c.-898C>A XP_011514056.1:n.-898C>A