Canonical Allele Identifier: CA1335317629
Gene: CHRNG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232543187G= , CM000664.2:g.232543187G= GRCh38
NC_000002.11:g.233407897G= , CM000664.1:g.233407897G= GRCh37
NC_000002.10:g.233116141G= NCBI36
NG_012954.1:g.8461G=
NG_012954.2:g.8496G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.806-88G= MANE Select ENSP00000498757.1:n.806-88G=
ENST00000389492.3:c.650-88G= ENSP00000374143.3:n.650-88G=
ENST00000389494.7:c.806-88G= ENSP00000374145.3:n.806-88G=
NM_005199.4:c.806-88G= NP_005190.4:n.806-88G=
NM_005199.5:c.806-88G= MANE Select NP_005190.4:n.806-88G=
Search 100 bp 5'
Search 100 bp 3'