Canonical Allele Identifier: CA397786101
Gene: CHRNB1 HGNC NCBI

Linked Data

dbSNP Id: rs912182651
gnomAD v2: 17-7348449-G-T
gnomAD v4: 17-7445130-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7445130G>T , CM000679.2:g.7445130G>T GRCh38
NC_000017.10:g.7348449G>T , CM000679.1:g.7348449G>T GRCh37
NC_000017.9:g.7289173G>T NCBI36
NG_008026.1:g.5044G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000306071.7:c.3G>T MANE Select ENSP00000304290.2:p.Met1Ile
ENST00000306071.6:c.3G>T ENSP00000304290.2:p.Met1Ile
ENST00000572857.5:c.3G>T ENSP00000461402.1:p.Met1Ile
ENST00000574054.1:n.23G>T
NM_000747.2:c.3G>T NP_000738.2:p.Met1Ile
NM_000747.3:c.3G>T MANE Select NP_000738.2:p.Met1Ile