Canonical Allele Identifier: CA371102529

Gene: CHRNB3

Linked Data

• MyVariant Identifiers: chr8:g.42587662A>C (hg19) ; chr8:g.42732519A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42732519A>C , CM000670.2:g.42732519A>C	GRCh38
NC_000008.10:g.42587662A>C , CM000670.1:g.42587662A>C	GRCh37
NC_000008.9:g.42706819A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289957.3:c.1212A>C MANE Select	ENSP00000289957.2:p.Arg404Ser
ENST00000289957.2:c.1212A>C	ENSP00000289957.2:p.Arg404Ser
NM_000749.3:c.1212A>C	NP_000740.1:p.Arg404Ser
XM_011544390.1:c.825A>C	XP_011542692.1:p.Arg275Ser
NM_000749.4:c.1212A>C	NP_000740.1:p.Arg404Ser
NM_001347717.1:c.990A>C	NP_001334646.1:p.Arg330Ser
XM_011544390.2:c.825A>C	XP_011542692.1:p.Arg275Ser
NM_000749.5:c.1212A>C MANE Select	NP_000740.1:p.Arg404Ser
NM_001347717.2:c.990A>C	NP_001334646.1:p.Arg330Ser