Canonical Allele Identifier: CA262352012
Gene:

Linked Data

dbSNP Id: rs768610707
MyVariant Identifiers: chr14:g.62968348G>C (hg19) chr14:g.62501630G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.62501630G>C , CM000676.2:g.62501630G>C GRCh38
NC_000014.8:g.62968348G>C , CM000676.1:g.62968348G>C GRCh37
NC_000014.7:g.62038101G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943932.1:n.116-2411G>C
XR_943932.2:n.103-2411G>C
Search 100 bp 5'
Search 100 bp 3'