Canonical Allele Identifier: CA724645391
Gene: GAN HGNC NCBI

Linked Data

dbSNP Id: rs1169259857
MyVariant Identifiers: chr16:g.81348546G>A (hg19) chr16:g.81314941G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81314941G>A , CM000678.2:g.81314941G>A GRCh38
NC_000016.9:g.81348546G>A , CM000678.1:g.81348546G>A GRCh37
NC_000016.8:g.79906047G>A NCBI36
NG_009007.1:g.4976G>A , LRG_242:g.4976G>A

Transcript Alleles

HGVS Amino-acid Change
XM_017023734.1:c.-697G>A XP_016879223.1:n.-697G>A
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