Canonical Allele Identifier: CA2206404206
Gene:

Linked Data

dbSNP Id: rs1567323834
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9249550C>T , CM000678.2:g.9249550C>T GRCh38
NC_000016.9:g.9343407C>T , CM000678.1:g.9343407C>T GRCh37
NC_000016.8:g.9250908C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933054.1:n.70+64817C>T
Search 100 bp 5'
Search 100 bp 3'