Canonical Allele Identifier: CA1335317627
Gene: CHRNG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232543181A= , CM000664.2:g.232543181A= GRCh38
NC_000002.11:g.233407891A= , CM000664.1:g.233407891A= GRCh37
NC_000002.10:g.233116135A= NCBI36
NG_012954.1:g.8455A=
NG_012954.2:g.8490A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.806-94A= MANE Select ENSP00000498757.1:n.806-94A=
ENST00000389492.3:c.650-94A= ENSP00000374143.3:n.650-94A=
ENST00000389494.7:c.806-94A= ENSP00000374145.3:n.806-94A=
NM_005199.4:c.806-94A= NP_005190.4:n.806-94A=
NM_005199.5:c.806-94A= MANE Select NP_005190.4:n.806-94A=
Search 100 bp 5'
Search 100 bp 3'