Canonical Allele Identifier: CA14174725

Gene:

Linked Data

• dbSNP Id: rs11636705
• gnomAD v2: 15-96605912-C-T
• gnomAD v3: 15-96062683-C-T
• gnomAD v4: 15-96062683-C-T
• MyVariant Identifiers: chr15:g.96605912C>T (hg19) ; chr15:g.96062683C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.96062683C>T , CM000677.2:g.96062683C>T	GRCh38
NC_000015.9:g.96605912C>T , CM000677.1:g.96605912C>T	GRCh37
NC_000015.8:g.94406916C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_002957737.1:n.450+71799C>T