Canonical Allele Identifier: CA30837880
Gene: CHRNB2 HGNC NCBI

Linked Data

dbSNP Id: rs914584021
MyVariant Identifiers: chr1:g.154548719_154548720insGGCC (hg19) chr1:g.154576243_154576244insGGCC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154576243_154576244insGGCC , CM000663.2:g.154576243_154576244insGGCC GRCh38
NC_000001.10:g.154548719_154548720insGGCC , CM000663.1:g.154548719_154548720insGGCC GRCh37
NC_000001.9:g.152815343_152815344insGGCC NCBI36
NG_008027.1:g.13463_13464insGGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.*311_*312insGGCC MANE Select ENSP00000357461.3:n.*311_*312insGGCC
ENST00000636034.1:c.1505+315_1505+316insGGCC ENSP00000489703.1:n.1505+315_1505+316insGGCC
ENST00000637900.1:c.*311_*312insGGCC ENSP00000490474.1:n.*311_*312insGGCC
ENST00000368476.3:c.*311_*312insGGCC ENSP00000357461.3:n.*311_*312insGGCC
NM_000748.2:c.*311_*312insGGCC NP_000739.1:n.*311_*312insGGCC
XM_017000180.2:c.*311_*312insGGCC XP_016855669.1:n.*311_*312insGGCC
XR_001736952.2:n.2072_2073insGGCC
NM_000748.3:c.*311_*312insGGCC MANE Select NP_000739.1:n.*311_*312insGGCC
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