Canonical Allele Identifier: CA164948141
Gene: CFTR HGNC NCBI

Linked Data

dbSNP Id: rs916680388
MyVariant Identifiers: chr7:g.117479040T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117479040T>A , CM000669.2:g.117479040T>A GRCh38
NC_000007.13:g.117119094T>A , CM000669.1:g.117119094T>A GRCh37
NC_000007.12:g.116906330T>A NCBI36
NG_016465.4:g.18257T>A , LRG_663:g.18257T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-525-204T>A ENSP00000417012.1:n.-525-204T>A
ENST00000673785.1:c.-406+13209T>A ENSP00000501235.1:n.-406+13209T>A
ENST00000546407.1:n.166+3232T>A
XM_011515751.1:c.42-204T>A XP_011514053.1:n.42-204T>A
XM_011515752.1:c.42-204T>A XP_011514054.1:n.42-204T>A
XM_011515754.1:c.-1057T>A XP_011514056.1:n.-1057T>A
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