Canonical Allele Identifier: CA397802632
Gene: CHRNB1 HGNC NCBI

Linked Data

dbSNP Id: rs1597755409
MyVariant Identifiers: chr17:g.7359202T>G (hg19) chr17:g.7455883T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7455883T>G , CM000679.2:g.7455883T>G GRCh38
NC_000017.10:g.7359202T>G , CM000679.1:g.7359202T>G GRCh37
NC_000017.9:g.7299926T>G NCBI36
NG_008026.1:g.15797T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000306071.7:c.1307T>G MANE Select ENSP00000304290.2:p.Val436Gly
ENST00000306071.6:c.1307T>G ENSP00000304290.2:p.Val436Gly
ENST00000536404.6:c.1091T>G ENSP00000439209.2:p.Val364Gly
ENST00000575379.1:c.-86T>G ENSP00000461751.1:n.-86T>G
ENST00000576360.1:c.944T>G ENSP00000459092.1:p.Val315Gly
NM_000747.2:c.1307T>G NP_000738.2:p.Val436Gly
NM_000747.3:c.1307T>G MANE Select NP_000738.2:p.Val436Gly
Search 100 bp 5'
Search 100 bp 3'