Canonical Allele Identifier: CA397297397
Gene: CHRNE HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.4802080T>G (hg19) chr17:g.4898785T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898785T>G , CM000679.2:g.4898785T>G GRCh38
NC_000017.10:g.4802080T>G , CM000679.1:g.4802080T>G GRCh37
NC_000017.9:g.4742859T>G NCBI36
NG_008029.2:g.9291A>C
NG_028005.1:g.70446T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.1433A>C MANE Select ENSP00000497829.1:p.Tyr478Ser
ENST00000649830.1:c.*69A>C ENSP00000496907.1:n.*69A>C
ENST00000652550.1:n.1159A>C
ENST00000293780.4:c.1433A>C ENSP00000293780.4:p.Tyr478Ser
ENST00000572438.1:n.1119A>C
NM_000080.3:c.1433A>C NP_000071.1:p.Tyr478Ser
NM_000080.4:c.1433A>C MANE Select NP_000071.1:p.Tyr478Ser
XM_017024115.1:c.1397A>C XP_016879604.1:p.Tyr466Ser
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