Canonical Allele Identifier: CA1335316689
Gene: CHRNG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232541345T= , CM000664.2:g.232541345T= GRCh38
NC_000002.11:g.233406055T= , CM000664.1:g.233406055T= GRCh37
NC_000002.10:g.233114299T= NCBI36
NG_012954.1:g.6619T=
NG_012954.2:g.6654T=

Transcript Alleles

HGVS Amino-acid change
ENST00000651502.1:c.351-29T= MANE Select ENSP00000498757.1:n.351-29T=
ENST00000389492.3:c.350+634T= ENSP00000374143.3:n.350+634T=
ENST00000389494.7:c.351-29T= ENSP00000374145.3:n.351-29T=
ENST00000485094.1:n.372-29T=
NM_005199.4:c.351-29T= NP_005190.4:n.351-29T=
NM_005199.5:c.351-29T= MANE Select NP_005190.4:n.351-29T=
Search 100 bp 5'
Search 100 bp 3'