Canonical Allele Identifier: CA2663621393
Gene: CHRNG HGNC NCBI

Linked Data

gnomAD v4: 2-232539785-TGCTG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232539790_232539793del , CM000664.2:g.232539790_232539793del GRCh38
NC_000002.11:g.233404500_233404503del , CM000664.1:g.233404500_233404503del GRCh37
NC_000002.10:g.233112744_233112747del NCBI36
NG_012954.1:g.5064_5067del
NG_012954.2:g.5099_5102del

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.43_46del MANE Select ENSP00000498757.1:p.Ala15SerfsTer18
ENST00000389492.3:c.43_46del ENSP00000374143.3:p.Ala15SerfsTer18
ENST00000389494.7:c.43_46del ENSP00000374145.3:p.Ala15SerfsTer18
ENST00000485094.1:n.64_67del
NM_005199.4:c.43_46del NP_005190.4:p.Ala15SerfsTer18
NM_005199.5:c.43_46del MANE Select NP_005190.4:p.Ala15SerfsTer18
Search 100 bp 5'
Search 100 bp 3'