Canonical Allele Identifier: CA356705677
Gene: CHRNA9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.40356173T>C (hg19) chr4:g.40354156T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354156T>C , CM000666.2:g.40354156T>C GRCh38
NC_000004.11:g.40356173T>C , CM000666.1:g.40356173T>C GRCh37
NC_000004.10:g.40050930T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310169.3:c.1076T>C MANE Select ENSP00000312663.2:p.Leu359Pro
ENST00000310169.2:c.1076T>C ENSP00000312663.2:p.Leu359Pro
NM_017581.3:c.1076T>C NP_060051.2:p.Leu359Pro
NM_017581.4:c.1076T>C MANE Select NP_060051.2:p.Leu359Pro
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