Canonical Allele Identifier: CA2635576081
Gene: CHRNE HGNC NCBI

Linked Data

gnomAD v4: 17-4898064-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898064C>T , CM000679.2:g.4898064C>T GRCh38
NC_000017.10:g.4801359C>T , CM000679.1:g.4801359C>T GRCh37
NC_000017.9:g.4742138C>T NCBI36
NG_008029.2:g.10012G>A
NG_028005.1:g.69725C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.*672G>A MANE Select ENSP00000497829.1:n.*672G>A
ENST00000652550.1:n.1880G>A
ENST00000293780.4:c.*672G>A ENSP00000293780.4:n.*672G>A
ENST00000572438.1:n.1840G>A
NM_000080.3:c.*672G>A NP_000071.1:n.*672G>A
NM_000080.4:c.*672G>A MANE Select NP_000071.1:n.*672G>A
XM_017024115.1:c.*672G>A XP_016879604.1:n.*672G>A
Search 100 bp 5'
Search 100 bp 3'