Canonical Allele Identifier: CA2635577154
Gene: CHRNE HGNC NCBI

Linked Data

gnomAD v4: 17-4898571-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898571C>T , CM000679.2:g.4898571C>T GRCh38
NC_000017.10:g.4801866C>T , CM000679.1:g.4801866C>T GRCh37
NC_000017.9:g.4742645C>T NCBI36
NG_008029.2:g.9505G>A
NG_028005.1:g.70232C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.*165G>A MANE Select ENSP00000497829.1:n.*165G>A
ENST00000649830.1:c.*283G>A ENSP00000496907.1:n.*283G>A
ENST00000652550.1:n.1373G>A
ENST00000293780.4:c.*165G>A ENSP00000293780.4:n.*165G>A
ENST00000572438.1:n.1333G>A
NM_000080.3:c.*165G>A NP_000071.1:n.*165G>A
NM_000080.4:c.*165G>A MANE Select NP_000071.1:n.*165G>A
XM_017024115.1:c.*165G>A XP_016879604.1:n.*165G>A
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