Canonical Allele Identifier: CA356707481
Gene: CHRNA9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354417G>C , CM000666.2:g.40354417G>C GRCh38
NC_000004.11:g.40356434G>C , CM000666.1:g.40356434G>C GRCh37
NC_000004.10:g.40051191G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000310169.3:c.1337G>C MANE Select ENSP00000312663.2:p.Ser446Thr
ENST00000310169.2:c.1337G>C ENSP00000312663.2:p.Ser446Thr
NM_017581.3:c.1337G>C NP_060051.2:p.Ser446Thr
NM_017581.4:c.1337G>C MANE Select NP_060051.2:p.Ser446Thr