Canonical Allele Identifier: CA1335317622
Gene: CHRNG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232543172T= , CM000664.2:g.232543172T= GRCh38
NC_000002.11:g.233407882T= , CM000664.1:g.233407882T= GRCh37
NC_000002.10:g.233116126T= NCBI36
NG_012954.1:g.8446T=
NG_012954.2:g.8481T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.805+90T= MANE Select ENSP00000498757.1:n.805+90T=
ENST00000389492.3:c.649+90T= ENSP00000374143.3:n.649+90T=
ENST00000389494.7:c.805+90T= ENSP00000374145.3:n.805+90T=
NM_005199.4:c.805+90T= NP_005190.4:n.805+90T=
NM_005199.5:c.805+90T= MANE Select NP_005190.4:n.805+90T=
Search 100 bp 5'
Search 100 bp 3'