Canonical Allele Identifier: CA342630209

Gene: CHRNB2

Linked Data

• MyVariant Identifiers: chr1:g.154543814A>T (hg19) ; chr1:g.154571338A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571338A>T , CM000663.2:g.154571338A>T	GRCh38
NC_000001.10:g.154543814A>T , CM000663.1:g.154543814A>T	GRCh37
NC_000001.9:g.152810438A>T	NCBI36
NG_008027.1:g.8558A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.515A>T MANE Select	ENSP00000357461.3:p.Lys172Met
ENST00000636034.1:c.515A>T	ENSP00000489703.1:p.Lys172Met
ENST00000637900.1:c.521A>T	ENSP00000490474.1:p.Lys174Met
ENST00000368476.3:c.515A>T	ENSP00000357461.3:p.Lys172Met
NM_000748.2:c.515A>T	NP_000739.1:p.Lys172Met
XM_017000180.2:c.5A>T	XP_016855669.1:p.Lys2Met
XR_001736952.2:n.767A>T
NM_000748.3:c.515A>T MANE Select	NP_000739.1:p.Lys172Met