Canonical Allele Identifier: CA1737344022
Gene: CFTR HGNC NCBI

Linked Data

dbSNP Id: rs1797959529
gnomAD v4: 7-117479570-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117479570C>A , CM000669.2:g.117479570C>A GRCh38
NC_000007.13:g.117119624C>A , CM000669.1:g.117119624C>A GRCh37
NC_000007.12:g.116906860C>A NCBI36
NG_016465.4:g.18787C>A , LRG_663:g.18787C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-315C>A ENSP00000417012.1:n.-315C>A
ENST00000673785.1:c.-406+13739C>A ENSP00000501235.1:n.-406+13739C>A
ENST00000446805.1:c.-315C>A ENSP00000417012.1:n.-315C>A
ENST00000546407.1:n.166+3762C>A
XM_011515751.1:c.143+225C>A XP_011514053.1:n.143+225C>A
XM_011515752.1:c.143+225C>A XP_011514054.1:n.143+225C>A
XM_011515753.1:c.-315C>A XP_011514055.1:n.-315C>A
XM_011515754.1:c.-643C>A XP_011514056.1:n.-643C>A
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