Canonical Allele Identifier: CA262352008

Gene:

Linked Data

• dbSNP Id: rs775229066
• gnomAD v3: 14-62501602-T-C
• gnomAD v4: 14-62501602-T-C
• MyVariant Identifiers: chr14:g.62968320T>C (hg19) ; chr14:g.62501602T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.62501602T>C , CM000676.2:g.62501602T>C	GRCh38
NC_000014.8:g.62968320T>C , CM000676.1:g.62968320T>C	GRCh37
NC_000014.7:g.62038073T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_943932.1:n.116-2439T>C
XR_943932.2:n.103-2439T>C