Canonical Allele Identifier: CA351008299
Gene: CHRNG HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.233406089A>C (hg19) chr2:g.232541379A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232541379A>C , CM000664.2:g.232541379A>C GRCh38
NC_000002.11:g.233406089A>C , CM000664.1:g.233406089A>C GRCh37
NC_000002.10:g.233114333A>C NCBI36
NG_012954.1:g.6653A>C
NG_012954.2:g.6688A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.356A>C MANE Select ENSP00000498757.1:p.Asp119Ala
ENST00000389492.3:c.350+668A>C ENSP00000374143.3:n.350+668A>C
ENST00000389494.7:c.356A>C ENSP00000374145.3:p.Asp119Ala
ENST00000485094.1:n.377A>C
NM_005199.4:c.356A>C NP_005190.4:p.Asp119Ala
NM_005199.5:c.356A>C MANE Select NP_005190.4:p.Asp119Ala
Search 100 bp 5'
Search 100 bp 3'