Canonical Allele Identifier: CA164948270

Gene: CFTR

Linked Data

• dbSNP Id: rs956742770
• MyVariant Identifiers: chr7:g.117119335A>G (hg19) ; chr7:g.117479281A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117479281A>G , CM000669.2:g.117479281A>G	GRCh38
NC_000007.13:g.117119335A>G , CM000669.1:g.117119335A>G	GRCh37
NC_000007.12:g.116906571A>G	NCBI36
NG_016465.4:g.18498A>G , LRG_663:g.18498A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446805.2:c.-488A>G	ENSP00000417012.1:n.-488A>G
ENST00000673785.1:c.-406+13450A>G	ENSP00000501235.1:n.-406+13450A>G
ENST00000546407.1:n.166+3473A>G
XM_011515751.1:c.79A>G	XP_011514053.1:p.Thr27Ala
XM_011515752.1:c.79A>G	XP_011514054.1:p.Thr27Ala
XM_011515754.1:c.-816A>G	XP_011514056.1:n.-816A>G