Canonical Allele Identifier: CA577211682
Gene: CFTR HGNC NCBI

Linked Data

dbSNP Id: rs1281407871
gnomAD v2: 7-117119586-G-T
gnomAD v3: 7-117479532-G-T
gnomAD v4: 7-117479532-G-T
MyVariant Identifiers: chr7:g.117119586G>T (hg19) chr7:g.117479532G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117479532G>T , CM000669.2:g.117479532G>T GRCh38
NC_000007.13:g.117119586G>T , CM000669.1:g.117119586G>T GRCh37
NC_000007.12:g.116906822G>T NCBI36
NG_016465.4:g.18749G>T , LRG_663:g.18749G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-353G>T ENSP00000417012.1:n.-353G>T
ENST00000673785.1:c.-406+13701G>T ENSP00000501235.1:n.-406+13701G>T
ENST00000446805.1:c.-353G>T ENSP00000417012.1:n.-353G>T
ENST00000546407.1:n.166+3724G>T
XM_011515751.1:c.143+187G>T XP_011514053.1:n.143+187G>T
XM_011515752.1:c.143+187G>T XP_011514054.1:n.143+187G>T
XM_011515753.1:c.-353G>T XP_011514055.1:n.-353G>T
XM_011515754.1:c.-681G>T XP_011514056.1:n.-681G>T
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