Canonical Allele Identifier: CA268552434
Gene: CHRNA7 HGNC NCBI

Linked Data

dbSNP Id: rs3087454
MyVariant Identifiers: chr15:g.32320967C>G (hg19) chr15:g.32028764C>G (hg38)
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Genomic Alleles

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

Transcript Alleles

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