Canonical Allele Identifier: CA1737343559
Gene: CFTR HGNC NCBI

Linked Data

dbSNP Id: rs1797934201

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117478942A>C , CM000669.2:g.117478942A>C GRCh38
NC_000007.13:g.117118996A>C , CM000669.1:g.117118996A>C GRCh37
NC_000007.12:g.116906232A>C NCBI36
NG_016465.4:g.18159A>C , LRG_663:g.18159A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-525-302A>C ENSP00000417012.1:n.-525-302A>C
ENST00000673785.1:c.-406+13111A>C ENSP00000501235.1:n.-406+13111A>C
ENST00000546407.1:n.166+3134A>C
XM_011515751.1:c.42-302A>C XP_011514053.1:n.42-302A>C
XM_011515752.1:c.42-302A>C XP_011514054.1:n.42-302A>C
XM_011515754.1:c.-1155A>C XP_011514056.1:n.-1155A>C