Canonical Allele Identifier: CA8313829
Gene: CHRNE HGNC NCBI

Linked Data

ClinVar Variation Id: 749052
ClinVar RCV Id: RCV000925887
dbSNP Id: rs372792059
ExAC: 17:4802100 G / A
gnomAD v2: 17-4802100-G-A
gnomAD v3: 17-4898805-G-A
gnomAD v4: 17-4898805-G-A
MyVariant Identifiers: chr17:g.4802100G>A (hg19) chr17:g.4898805G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898805G>A , CM000679.2:g.4898805G>A GRCh38
NC_000017.10:g.4802100G>A , CM000679.1:g.4802100G>A GRCh37
NC_000017.9:g.4742879G>A NCBI36
NG_008029.2:g.9271C>T
NG_028005.1:g.70466G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.1413C>T MANE Select ENSP00000497829.1:p.Ser471=
ENST00000649830.1:c.*49C>T ENSP00000496907.1:n.*49C>T
ENST00000652550.1:n.1139C>T
ENST00000293780.4:c.1413C>T ENSP00000293780.4:p.Ser471=
ENST00000572438.1:n.1099C>T
NM_000080.3:c.1413C>T NP_000071.1:p.Ser471=
NM_000080.4:c.1413C>T MANE Select NP_000071.1:p.Ser471=
XM_017024115.1:c.1377C>T XP_016879604.1:p.Ser459=
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