Canonical Allele Identifier: CA832112563
Gene: CFTR HGNC NCBI

Linked Data

dbSNP Id: rs916784395
MyVariant Identifiers: chr7:g.117119657C>G (hg19) chr7:g.117479603C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117479603C>G , CM000669.2:g.117479603C>G GRCh38
NC_000007.13:g.117119657C>G , CM000669.1:g.117119657C>G GRCh37
NC_000007.12:g.116906893C>G NCBI36
NG_016465.4:g.18820C>G , LRG_663:g.18820C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-282C>G ENSP00000417012.1:n.-282C>G
ENST00000673785.1:c.-406+13772C>G ENSP00000501235.1:n.-406+13772C>G
ENST00000446805.1:c.-282C>G ENSP00000417012.1:n.-282C>G
ENST00000546407.1:n.166+3795C>G
XM_011515751.1:c.143+258C>G XP_011514053.1:n.143+258C>G
XM_011515752.1:c.143+258C>G XP_011514054.1:n.143+258C>G
XM_011515753.1:c.-282C>G XP_011514055.1:n.-282C>G
XM_011515754.1:c.-610C>G XP_011514056.1:n.-610C>G
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