Canonical Allele Identifier: CA2663621508
Gene: CHRNG HGNC NCBI

Linked Data

gnomAD v4: 2-232539905-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232539905T>G , CM000664.2:g.232539905T>G GRCh38
NC_000002.11:g.233404615T>G , CM000664.1:g.233404615T>G GRCh37
NC_000002.10:g.233112859T>G NCBI36
NG_012954.1:g.5179T>G
NG_012954.2:g.5214T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.56-87T>G MANE Select ENSP00000498757.1:n.56-87T>G
ENST00000389492.3:c.56-87T>G ENSP00000374143.3:n.56-87T>G
ENST00000389494.7:c.56-87T>G ENSP00000374145.3:n.56-87T>G
ENST00000485094.1:n.77-87T>G
NM_005199.4:c.56-87T>G NP_005190.4:n.56-87T>G
NM_005199.5:c.56-87T>G MANE Select NP_005190.4:n.56-87T>G
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