Canonical Allele Identifier: CA2635577406
Gene: CHRNE HGNC NCBI

Linked Data

gnomAD v4: 17-4898702-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898702C>T , CM000679.2:g.4898702C>T GRCh38
NC_000017.10:g.4801997C>T , CM000679.1:g.4801997C>T GRCh37
NC_000017.9:g.4742776C>T NCBI36
NG_008029.2:g.9374G>A
NG_028005.1:g.70363C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.*34G>A MANE Select ENSP00000497829.1:n.*34G>A
ENST00000649830.1:c.*152G>A ENSP00000496907.1:n.*152G>A
ENST00000652550.1:n.1242G>A
ENST00000293780.4:c.*34G>A ENSP00000293780.4:n.*34G>A
ENST00000572438.1:n.1202G>A
NM_000080.3:c.*34G>A NP_000071.1:n.*34G>A
NM_000080.4:c.*34G>A MANE Select NP_000071.1:n.*34G>A
XM_017024115.1:c.*34G>A XP_016879604.1:n.*34G>A
Search 100 bp 5'
Search 100 bp 3'