Canonical Allele Identifier: CA351008898
Gene: CHRNG HGNC NCBI

Linked Data

dbSNP Id: rs1692015613
gnomAD v4: 2-232541450-C-T
MyVariant Identifiers: chr2:g.233406160C>T (hg19) chr2:g.232541450C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232541450C>T , CM000664.2:g.232541450C>T GRCh38
NC_000002.11:g.233406160C>T , CM000664.1:g.233406160C>T GRCh37
NC_000002.10:g.233114404C>T NCBI36
NG_012954.1:g.6724C>T
NG_012954.2:g.6759C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.427C>T MANE Select ENSP00000498757.1:p.Pro143Ser
ENST00000389492.3:c.350+739C>T ENSP00000374143.3:n.350+739C>T
ENST00000389494.7:c.427C>T ENSP00000374145.3:p.Pro143Ser
ENST00000485094.1:n.448C>T
NM_005199.4:c.427C>T NP_005190.4:p.Pro143Ser
NM_005199.5:c.427C>T MANE Select NP_005190.4:p.Pro143Ser
Search 100 bp 5'
Search 100 bp 3'