Canonical Allele Identifier: CA287177924
Gene: CHRNE HGNC NCBI

Linked Data

dbSNP Id: rs996379460
MyVariant Identifiers: chr17:g.4801426G>C (hg19) chr17:g.4898131G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898131G>C , CM000679.2:g.4898131G>C GRCh38
NC_000017.10:g.4801426G>C , CM000679.1:g.4801426G>C GRCh37
NC_000017.9:g.4742205G>C NCBI36
NG_008029.2:g.9945C>G
NG_028005.1:g.69792G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.*605C>G MANE Select ENSP00000497829.1:n.*605C>G
ENST00000649830.1:c.*723C>G ENSP00000496907.1:n.*723C>G
ENST00000652550.1:n.1813C>G
ENST00000293780.4:c.*605C>G ENSP00000293780.4:n.*605C>G
ENST00000572438.1:n.1773C>G
NM_000080.3:c.*605C>G NP_000071.1:n.*605C>G
NM_000080.4:c.*605C>G MANE Select NP_000071.1:n.*605C>G
XM_017024115.1:c.*605C>G XP_016879604.1:n.*605C>G
Search 100 bp 5'
Search 100 bp 3'