Canonical Allele Identifier: CA164948023
Gene: CFTR HGNC NCBI

Linked Data

dbSNP Id: rs989782130
gnomAD v3: 7-117478808-G-A
gnomAD v4: 7-117478808-G-A
MyVariant Identifiers: chr7:g.117118862G>A (hg19) chr7:g.117478808G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117478808G>A , CM000669.2:g.117478808G>A GRCh38
NC_000007.13:g.117118862G>A , CM000669.1:g.117118862G>A GRCh37
NC_000007.12:g.116906098G>A NCBI36
NG_016465.4:g.18025G>A , LRG_663:g.18025G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-526+386G>A ENSP00000417012.1:n.-526+386G>A
ENST00000673785.1:c.-406+12977G>A ENSP00000501235.1:n.-406+12977G>A
ENST00000546407.1:n.166+3000G>A
XM_011515751.1:c.41+386G>A XP_011514053.1:n.41+386G>A
XM_011515752.1:c.41+386G>A XP_011514054.1:n.41+386G>A
XM_011515754.1:c.-1289G>A XP_011514056.1:n.-1289G>A
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