Canonical Allele Identifier: CA2480927270
Gene: CHRNB2 HGNC NCBI

Linked Data

dbSNP Id: rs1696269425
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154576074dup , CM000663.2:g.154576074dup GRCh38
NC_000001.10:g.154548550dup , CM000663.1:g.154548550dup GRCh37
NC_000001.9:g.152815174dup NCBI36
NG_008027.1:g.13294dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.*142dup MANE Select ENSP00000357461.3:n.*142dup
ENST00000636034.1:c.1505+146dup ENSP00000489703.1:n.1505+146dup
ENST00000637900.1:c.*142dup ENSP00000490474.1:n.*142dup
ENST00000368476.3:c.*142dup ENSP00000357461.3:n.*142dup
NM_000748.2:c.*142dup NP_000739.1:n.*142dup
XM_017000180.2:c.*142dup XP_016855669.1:n.*142dup
XR_001736952.2:n.1903dup
NM_000748.3:c.*142dup MANE Select NP_000739.1:n.*142dup
Search 100 bp 5'
Search 100 bp 3'