Canonical Allele Identifier: CA577211704
Gene: CFTR HGNC NCBI

Linked Data

dbSNP Id: rs1410587639
gnomAD v2: 7-117119740-T-G
gnomAD v3: 7-117479686-T-G
gnomAD v4: 7-117479686-T-G
MyVariant Identifiers: chr7:g.117119740T>G (hg19) chr7:g.117479686T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117479686T>G , CM000669.2:g.117479686T>G GRCh38
NC_000007.13:g.117119740T>G , CM000669.1:g.117119740T>G GRCh37
NC_000007.12:g.116906976T>G NCBI36
NG_016465.4:g.18903T>G , LRG_663:g.18903T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-199T>G ENSP00000417012.1:n.-199T>G
ENST00000673785.1:c.-406+13855T>G ENSP00000501235.1:n.-406+13855T>G
ENST00000446805.1:c.-199T>G ENSP00000417012.1:n.-199T>G
ENST00000546407.1:n.166+3878T>G
XM_011515751.1:c.143+341T>G XP_011514053.1:n.143+341T>G
XM_011515752.1:c.143+341T>G XP_011514054.1:n.143+341T>G
XM_011515753.1:c.-199T>G XP_011514055.1:n.-199T>G
XM_011515754.1:c.-527T>G XP_011514056.1:n.-527T>G
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