Canonical Allele Identifier: CA497675745
Gene: CHRNE HGNC NCBI

Linked Data

ClinVar Variation Id: 1129734
ClinVar RCV Id: RCV001462954
dbSNP Id: rs950225592
gnomAD v4: 17-4898751-C-A
MyVariant Identifiers: chr17:g.4802046C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898751C>A , CM000679.2:g.4898751C>A GRCh38
NC_000017.10:g.4802046C>A , CM000679.1:g.4802046C>A GRCh37
NC_000017.9:g.4742825C>A NCBI36
NG_008029.2:g.9325G>T
NG_028005.1:g.70412C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.1467G>T MANE Select ENSP00000497829.1:p.Pro489=
ENST00000649830.1:c.*103G>T ENSP00000496907.1:n.*103G>T
ENST00000652550.1:n.1193G>T
ENST00000293780.4:c.1467G>T ENSP00000293780.4:p.Pro489=
ENST00000572438.1:n.1153G>T
NM_000080.3:c.1467G>T NP_000071.1:p.Pro489=
NM_000080.4:c.1467G>T MANE Select NP_000071.1:p.Pro489=
XM_017024115.1:c.1431G>T XP_016879604.1:p.Pro477=
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