Canonical Allele Identifier: CA356706577
Gene: CHRNA9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354315A>T , CM000666.2:g.40354315A>T GRCh38
NC_000004.11:g.40356332A>T , CM000666.1:g.40356332A>T GRCh37
NC_000004.10:g.40051089A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000310169.3:c.1235A>T MANE Select ENSP00000312663.2:p.Gln412Leu
ENST00000310169.2:c.1235A>T ENSP00000312663.2:p.Gln412Leu
NM_017581.3:c.1235A>T NP_060051.2:p.Gln412Leu
NM_017581.4:c.1235A>T MANE Select NP_060051.2:p.Gln412Leu