Canonical Allele Identifier: CA356708163
Gene: CHRNA9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.40356455A>C (hg19) chr4:g.40354438A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354438A>C , CM000666.2:g.40354438A>C GRCh38
NC_000004.11:g.40356455A>C , CM000666.1:g.40356455A>C GRCh37
NC_000004.10:g.40051212A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000310169.3:c.1358A>C MANE Select ENSP00000312663.2:p.Lys453Thr
ENST00000310169.2:c.1358A>C ENSP00000312663.2:p.Lys453Thr
NM_017581.3:c.1358A>C NP_060051.2:p.Lys453Thr
NM_017581.4:c.1358A>C MANE Select NP_060051.2:p.Lys453Thr
Search 100 bp 5'
Search 100 bp 3'