Canonical Allele Identifier: CA356707473

Gene: CHRNA9

Linked Data

• MyVariant Identifiers: chr4:g.40356431G>T (hg19) ; chr4:g.40354414G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.40354414G>T , CM000666.2:g.40354414G>T	GRCh38
NC_000004.11:g.40356431G>T , CM000666.1:g.40356431G>T	GRCh37
NC_000004.10:g.40051188G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000310169.3:c.1334G>T MANE Select	ENSP00000312663.2:p.Gly445Val
ENST00000310169.2:c.1334G>T	ENSP00000312663.2:p.Gly445Val
NM_017581.3:c.1334G>T	NP_060051.2:p.Gly445Val
NM_017581.4:c.1334G>T MANE Select	NP_060051.2:p.Gly445Val