Canonical Allele Identifier: CA397297231
Gene: CHRNE HGNC NCBI

Linked Data

dbSNP Id: rs373293781
MyVariant Identifiers: chr17:g.4802052G>C (hg19) chr17:g.4898757G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898757G>C , CM000679.2:g.4898757G>C GRCh38
NC_000017.10:g.4802052G>C , CM000679.1:g.4802052G>C GRCh37
NC_000017.9:g.4742831G>C NCBI36
NG_008029.2:g.9319C>G
NG_028005.1:g.70418G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.1461C>G MANE Select ENSP00000497829.1:p.Tyr487Ter
ENST00000649830.1:c.*97C>G ENSP00000496907.1:n.*97C>G
ENST00000652550.1:n.1187C>G
ENST00000293780.4:c.1461C>G ENSP00000293780.4:p.Tyr487Ter
ENST00000572438.1:n.1147C>G
NM_000080.3:c.1461C>G NP_000071.1:p.Tyr487Ter
NM_000080.4:c.1461C>G MANE Select NP_000071.1:p.Tyr487Ter
XM_017024115.1:c.1425C>G XP_016879604.1:p.Tyr475Ter
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