Canonical Allele Identifier: CA2244610291

Gene: CHRNE

Linked Data

• dbSNP Id: rs371649855

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4898712G>C , CM000679.2:g.4898712G>C	GRCh38
NC_000017.10:g.4802007G>C , CM000679.1:g.4802007G>C	GRCh37
NC_000017.9:g.4742786G>C	NCBI36
NG_008029.2:g.9364C>G
NG_028005.1:g.70373G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649488.2:c.*24C>G MANE Select	ENSP00000497829.1:n.*24C>G
ENST00000649830.1:c.*142C>G	ENSP00000496907.1:n.*142C>G
ENST00000652550.1:n.1232C>G
ENST00000293780.4:c.*24C>G	ENSP00000293780.4:n.*24C>G
ENST00000572438.1:n.1192C>G
NM_000080.3:c.*24C>G	NP_000071.1:n.*24C>G
NM_000080.4:c.*24C>G MANE Select	NP_000071.1:n.*24C>G
XM_017024115.1:c.*24C>G	XP_016879604.1:n.*24C>G