Canonical Allele Identifier: CA725798549
Gene:

Linked Data

dbSNP Id: rs921774543
MyVariant Identifiers: chr16:g.9343541T>C (hg19) chr16:g.9249684T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9249684T>C , CM000678.2:g.9249684T>C GRCh38
NC_000016.9:g.9343541T>C , CM000678.1:g.9343541T>C GRCh37
NC_000016.8:g.9251042T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933054.1:n.70+64951T>C
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