Canonical Allele Identifier: CA2168250214
Gene: CHRNA7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.32028719C= , CM000677.2:g.32028719C= GRCh38
NC_000015.9:g.32320922C= , CM000677.1:g.32320922C= GRCh37
NC_000015.8:g.30108214C= NCBI36
NG_009216.1:g.3197C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000635978.1:c.-42-72584C= ENSP00000490778.1:n.-42-72584C=
ENST00000636603.1:c.-131-2179C= ENSP00000490513.1:n.-131-2179C=
ENST00000637183.1:c.-43+50525C= ENSP00000490365.1:n.-43+50525C=
ENST00000638106.1:c.-378-2179C= ENSP00000490413.1:n.-378-2179C=
XM_011522320.1:c.573-112G= XP_011520622.1:n.573-112G=
XM_011522320.2:c.573-112G= XP_011520622.1:n.573-112G=