Canonical Allele Identifier: CA438955691
Gene: CHRNA9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.40356531G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354514G>C , CM000666.2:g.40354514G>C GRCh38
NC_000004.11:g.40356531G>C , CM000666.1:g.40356531G>C GRCh37
NC_000004.10:g.40051288G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310169.3:c.1434G>C MANE Select ENSP00000312663.2:p.Ala478=
ENST00000310169.2:c.1434G>C ENSP00000312663.2:p.Ala478=
NM_017581.3:c.1434G>C NP_060051.2:p.Ala478=
NM_017581.4:c.1434G>C MANE Select NP_060051.2:p.Ala478=