Canonical Allele Identifier: CA265581626
Gene:

Linked Data

dbSNP Id: rs752425459
MyVariant Identifiers: chr14:g.92781065G>C (hg19) chr14:g.92314721G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92314721G>C , CM000676.2:g.92314721G>C GRCh38
NC_000014.8:g.92781065G>C , CM000676.1:g.92781065G>C GRCh37
NC_000014.7:g.91850818G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944153.1:n.132-525G>C
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