Canonical Allele Identifier: CA1737344157
Gene: CFTR HGNC NCBI

Linked Data

dbSNP Id: rs1797964564
gnomAD v4: 7-117479739-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117479739T>C , CM000669.2:g.117479739T>C GRCh38
NC_000007.13:g.117119793T>C , CM000669.1:g.117119793T>C GRCh37
NC_000007.12:g.116907029T>C NCBI36
NG_016465.4:g.18956T>C , LRG_663:g.18956T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000446805.2:c.-191+45T>C ENSP00000417012.1:n.-191+45T>C
ENST00000673785.1:c.-406+13908T>C ENSP00000501235.1:n.-406+13908T>C
ENST00000446805.1:c.-191+45T>C ENSP00000417012.1:n.-191+45T>C
ENST00000546407.1:n.166+3931T>C
XM_011515751.1:c.143+394T>C XP_011514053.1:n.143+394T>C
XM_011515752.1:c.143+394T>C XP_011514054.1:n.143+394T>C
XM_011515753.1:c.-191+45T>C XP_011514055.1:n.-191+45T>C
XM_011515754.1:c.-519+45T>C XP_011514056.1:n.-519+45T>C
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