Canonical Allele Identifier: CA2635579107
Gene: CHRNE HGNC NCBI

Linked Data

gnomAD v4: 17-4899412-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4899412G>A , CM000679.2:g.4899412G>A GRCh38
NC_000017.10:g.4802707G>A , CM000679.1:g.4802707G>A GRCh37
NC_000017.9:g.4743486G>A NCBI36
NG_008029.2:g.8664C>T
NG_028005.1:g.71073G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.1033-28C>T MANE Select ENSP00000497829.1:n.1033-28C>T
ENST00000649830.1:c.100-28C>T ENSP00000496907.1:n.100-28C>T
ENST00000652550.1:n.763-28C>T
ENST00000293780.4:c.1033-28C>T ENSP00000293780.4:n.1033-28C>T
ENST00000572438.1:n.719-28C>T
NM_000080.3:c.1033-28C>T NP_000071.1:n.1033-28C>T
NM_000080.4:c.1033-28C>T MANE Select NP_000071.1:n.1033-28C>T
XM_017024115.1:c.997-28C>T XP_016879604.1:n.997-28C>T
XR_001752421.1:n.1763-28C>T