Canonical Allele Identifier: CA356708776

Gene: CHRNA9

Linked Data

• MyVariant Identifiers: chr4:g.40356532G>C (hg19) ; chr4:g.40354515G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.40354515G>C , CM000666.2:g.40354515G>C	GRCh38
NC_000004.11:g.40356532G>C , CM000666.1:g.40356532G>C	GRCh37
NC_000004.10:g.40051289G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310169.3:c.1435G>C MANE Select	ENSP00000312663.2:p.Asp479His
ENST00000310169.2:c.1435G>C	ENSP00000312663.2:p.Asp479His
NM_017581.3:c.1435G>C	NP_060051.2:p.Asp479His
NM_017581.4:c.1435G>C MANE Select	NP_060051.2:p.Asp479His