Canonical Allele Identifier: CA397786086
Gene: CHRNB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7445128A>C , CM000679.2:g.7445128A>C GRCh38
NC_000017.10:g.7348447A>C , CM000679.1:g.7348447A>C GRCh37
NC_000017.9:g.7289171A>C NCBI36
NG_008026.1:g.5042A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000306071.7:c.1A>C MANE Select ENSP00000304290.2:p.Met1Leu
ENST00000306071.6:c.1A>C ENSP00000304290.2:p.Met1Leu
ENST00000572857.5:c.1A>C ENSP00000461402.1:p.Met1Leu
ENST00000574054.1:n.21A>C
NM_000747.2:c.1A>C NP_000738.2:p.Met1Leu
NM_000747.3:c.1A>C MANE Select NP_000738.2:p.Met1Leu