Canonical Allele Identifier: CA284263999
Gene: GAN HGNC NCBI

Linked Data

dbSNP Id: rs552228941
gnomAD v3: 16-81314959-C-A
gnomAD v4: 16-81314959-C-A
MyVariant Identifiers: chr16:g.81348564C>A (hg19) chr16:g.81314959C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81314959C>A , CM000678.2:g.81314959C>A GRCh38
NC_000016.9:g.81348564C>A , CM000678.1:g.81348564C>A GRCh37
NC_000016.8:g.79906065C>A NCBI36
NG_009007.1:g.4994C>A , LRG_242:g.4994C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000648349.2:c.-155C>A ENSP00000498114.1:n.-155C>A
ENST00000568107.2:c.-155C>A ENSP00000476795.1:n.-155C>A
XM_017023734.1:c.-679C>A XP_016879223.1:n.-679C>A
Search 100 bp 5'
Search 100 bp 3'