Canonical Allele Identifier: CA497675698
Gene: CHRNE HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.4802012A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898717A>G , CM000679.2:g.4898717A>G GRCh38
NC_000017.10:g.4802012A>G , CM000679.1:g.4802012A>G GRCh37
NC_000017.9:g.4742791A>G NCBI36
NG_008029.2:g.9359T>C
NG_028005.1:g.70378A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.*19T>C MANE Select ENSP00000497829.1:n.*19T>C
ENST00000649830.1:c.*137T>C ENSP00000496907.1:n.*137T>C
ENST00000652550.1:n.1227T>C
ENST00000293780.4:c.*19T>C ENSP00000293780.4:n.*19T>C
ENST00000572438.1:n.1187T>C
NM_000080.3:c.*19T>C NP_000071.1:n.*19T>C
NM_000080.4:c.*19T>C MANE Select NP_000071.1:n.*19T>C
XM_017024115.1:c.*19T>C XP_016879604.1:n.*19T>C
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