Canonical Allele Identifier: CA1737344359
Gene: CFTR HGNC NCBI

Linked Data

dbSNP Id: rs1797970579
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117479907G>A , CM000669.2:g.117479907G>A GRCh38
NC_000007.13:g.117119961G>A , CM000669.1:g.117119961G>A GRCh37
NC_000007.12:g.116907197G>A NCBI36
NG_016465.4:g.19124G>A , LRG_663:g.19124G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-191+213G>A ENSP00000417012.1:n.-191+213G>A
ENST00000673785.1:c.-406+14076G>A ENSP00000501235.1:n.-406+14076G>A
ENST00000446805.1:c.-191+213G>A ENSP00000417012.1:n.-191+213G>A
ENST00000546407.1:n.166+4099G>A
XM_011515751.1:c.143+562G>A XP_011514053.1:n.143+562G>A
XM_011515752.1:c.143+562G>A XP_011514054.1:n.143+562G>A
XM_011515753.1:c.-191+213G>A XP_011514055.1:n.-191+213G>A
XM_011515754.1:c.-519+213G>A XP_011514056.1:n.-519+213G>A
Search 100 bp 5'
Search 100 bp 3'