Canonical Allele Identifier: CA15806661

Gene:

Linked Data

• dbSNP Id: rs1676303
• gnomAD v2: 14-76992164-C-T
• gnomAD v3: 14-76525821-C-T
• gnomAD v4: 14-76525821-C-T
• MyVariant Identifiers: chr14:g.76992164C>T (hg19) ; chr14:g.76525821C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.76525821C>T , CM000676.2:g.76525821C>T	GRCh38
NC_000014.8:g.76992164C>T , CM000676.1:g.76992164C>T	GRCh37
NC_000014.7:g.76061917C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_944039.1:n.41-23561G>A