Canonical Allele Identifier: CA356705915
Gene: CHRNA9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354208A>T , CM000666.2:g.40354208A>T GRCh38
NC_000004.11:g.40356225A>T , CM000666.1:g.40356225A>T GRCh37
NC_000004.10:g.40050982A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310169.3:c.1128A>T MANE Select ENSP00000312663.2:p.Lys376Asn
ENST00000310169.2:c.1128A>T ENSP00000312663.2:p.Lys376Asn
NM_017581.3:c.1128A>T NP_060051.2:p.Lys376Asn
NM_017581.4:c.1128A>T MANE Select NP_060051.2:p.Lys376Asn