Canonical Allele Identifier: CA1106299737
Gene: CFTR HGNC NCBI

Linked Data

dbSNP Id: rs1797928789
gnomAD v3: 7-117478755-G-A
gnomAD v4: 7-117478755-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117478755G>A , CM000669.2:g.117478755G>A GRCh38
NC_000007.13:g.117118809G>A , CM000669.1:g.117118809G>A GRCh37
NC_000007.12:g.116906045G>A NCBI36
NG_016465.4:g.17972G>A , LRG_663:g.17972G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-526+333G>A ENSP00000417012.1:n.-526+333G>A
ENST00000673785.1:c.-406+12924G>A ENSP00000501235.1:n.-406+12924G>A
ENST00000546407.1:n.166+2947G>A
XM_011515751.1:c.41+333G>A XP_011514053.1:n.41+333G>A
XM_011515752.1:c.41+333G>A XP_011514054.1:n.41+333G>A
XM_011515754.1:c.-1342G>A XP_011514056.1:n.-1342G>A
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