Canonical Allele Identifier: CA1452583825
Gene: CHRNA9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354271C= , CM000666.2:g.40354271C= GRCh38
NC_000004.11:g.40356288C= , CM000666.1:g.40356288C= GRCh37
NC_000004.10:g.40051045C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310169.3:c.1191C= MANE Select ENSP00000312663.2:p.Asn397=
ENST00000310169.2:c.1191C= ENSP00000312663.2:p.Asn397=
NM_017581.3:c.1191C= NP_060051.2:p.Asn397=
NM_017581.4:c.1191C= MANE Select NP_060051.2:p.Asn397=
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