Canonical Allele Identifier: CA287177866
Gene: CHRNE HGNC NCBI

Linked Data

dbSNP Id: rs929739835

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898073T>G , CM000679.2:g.4898073T>G GRCh38
NC_000017.10:g.4801368T>G , CM000679.1:g.4801368T>G GRCh37
NC_000017.9:g.4742147T>G NCBI36
NG_008029.2:g.10003A>C
NG_028005.1:g.69734T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.*663A>C MANE Select ENSP00000497829.1:n.*663A>C
ENST00000652550.1:n.1871A>C
ENST00000293780.4:c.*663A>C ENSP00000293780.4:n.*663A>C
ENST00000572438.1:n.1831A>C
NM_000080.3:c.*663A>C NP_000071.1:n.*663A>C
NM_000080.4:c.*663A>C MANE Select NP_000071.1:n.*663A>C
XM_017024115.1:c.*663A>C XP_016879604.1:n.*663A>C