Canonical Allele Identifier: CA268552444

Gene: CHRNA7

Linked Data

• dbSNP Id: rs3087454
• MyVariant Identifiers: chr15:g.32320967C>T (hg19) ; chr15:g.32028764C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.32028764C>T , CM000677.2:g.32028764C>T	GRCh38
NC_000015.9:g.32320967C>T , CM000677.1:g.32320967C>T	GRCh37
NC_000015.8:g.30108259C>T	NCBI36
NG_009216.1:g.3242C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000635978.1:c.-42-72539C>T	ENSP00000490778.1:n.-42-72539C>T
ENST00000636603.1:c.-131-2134C>T	ENSP00000490513.1:n.-131-2134C>T
ENST00000637183.1:c.-43+50570C>T	ENSP00000490365.1:n.-43+50570C>T
ENST00000638106.1:c.-378-2134C>T	ENSP00000490413.1:n.-378-2134C>T
XM_011522320.1:c.573-157G>A	XP_011520622.1:n.573-157G>A
XM_011522320.2:c.573-157G>A	XP_011520622.1:n.573-157G>A