Canonical Allele Identifier: CA2244609837
Gene: CHRNE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898071C= , CM000679.2:g.4898071C= GRCh38
NC_000017.10:g.4801366C= , CM000679.1:g.4801366C= GRCh37
NC_000017.9:g.4742145C= NCBI36
NG_008029.2:g.10005G=
NG_028005.1:g.69732C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.*665G= MANE Select ENSP00000497829.1:n.*665G=
ENST00000652550.1:n.1873G=
ENST00000293780.4:c.*665G= ENSP00000293780.4:n.*665G=
ENST00000572438.1:n.1833G=
NM_000080.3:c.*665G= NP_000071.1:n.*665G=
NM_000080.4:c.*665G= MANE Select NP_000071.1:n.*665G=
XM_017024115.1:c.*665G= XP_016879604.1:n.*665G=
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