Canonical Allele Identifier: CA1737343370
Gene: CFTR HGNC NCBI

Linked Data

dbSNP Id: rs1797928515
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117478748C>T , CM000669.2:g.117478748C>T GRCh38
NC_000007.13:g.117118802C>T , CM000669.1:g.117118802C>T GRCh37
NC_000007.12:g.116906038C>T NCBI36
NG_016465.4:g.17965C>T , LRG_663:g.17965C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000446805.2:c.-526+326C>T ENSP00000417012.1:n.-526+326C>T
ENST00000673785.1:c.-406+12917C>T ENSP00000501235.1:n.-406+12917C>T
ENST00000546407.1:n.166+2940C>T
XM_011515751.1:c.41+326C>T XP_011514053.1:n.41+326C>T
XM_011515752.1:c.41+326C>T XP_011514054.1:n.41+326C>T
XM_011515754.1:c.-1349C>T XP_011514056.1:n.-1349C>T
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