Canonical Allele Identifier: CA2577278478
Gene: CHRNG HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232543169G>A , CM000664.2:g.232543169G>A GRCh38
NC_000002.11:g.233407879G>A , CM000664.1:g.233407879G>A GRCh37
NC_000002.10:g.233116123G>A NCBI36
NG_012954.1:g.8443G>A
NG_012954.2:g.8478G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.805+87G>A MANE Select ENSP00000498757.1:n.805+87G>A
ENST00000389492.3:c.649+87G>A ENSP00000374143.3:n.649+87G>A
ENST00000389494.7:c.805+87G>A ENSP00000374145.3:n.805+87G>A
NM_005199.4:c.805+87G>A NP_005190.4:n.805+87G>A
NM_005199.5:c.805+87G>A MANE Select NP_005190.4:n.805+87G>A
Search 100 bp 5'
Search 100 bp 3'